FDA 3644 Ultrasonic therapy (esubmitter)

Submission Report

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Submission Report
eRadHealth Menu
Introduction

Electronic Product Radiation Safety Reporting
Form
This software application is intended to automate the hard copy product reporting forms in the effort
of the Center for Devices and Radiological Health (CDRH) to become capable of accepting
electronic submissions from industry and to improve our review process. This FDA Electronic
Submission (eSub) software is the next version of the application developed to allow us to accept all
Radiological Health reports and other submissions electronically and improve the ability of CDRH
to accomplish its mandated product and industry evaluations in a timely and efficient manner.
All electronic reports and correspondence can either be transferred to CD and mailed to the address
below, or can be sent via the FDA Electronic Submissions Gateway to CDRH. If you follow
instructions to set up an account with the FDA Gateway, it currently may take several weeks,, but
when you submit through it you will receive your acknowledgement email message with Accession
Number within minutes! Or, in the interest of faster turn-around for a one-time urgent report of if
you submit few reports, you may simply fill out this template creating the submission and then at
'Packaging' follow the instructions to transfer the files to a CD to mail in. This method of submitting
your report will be acknowledged by an email with the Accession Number within several days.
Information about the FDA Electronic Submissions Gateway can be found at
www.fda.gov/ForIndustry/ElectronicSubmissionsGateway/default.htm. Please contact the
Gateway Helpdesk with your questions about that system.
Electronic submissions on CD should be mailed directly to the Document Control Center at:
U.S. Food and Drug Administration
Center for Devices and Radiological Health
Attn: eSubmitter Team
Document Mail Center - WO66-0609
10903 New Hampshire Avenue
Silver Spring, MD 20993-0002
Submissions received in the mail on CD will be processed within a few days of receipt.
Note about eSubmitter software:
Instructions provided in this software briefly summarize the requirements of the regulations under
the Federal Food, Drug and Cosmetic Act (FFDCA), Chapter V, Subchapter C - Electronic Product

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Radiation Control, that applies to manufacturers of electronic products that emit radiation. The
software provides questions relevant to requirements in the performance standards and may include
explanations or clarification about the performance, labeling, and informational requirements of the
standard. It does not replace the regulations, however, and if there is any conflict between the
software and the regulations, the regulations must prevail. Throughout this application, pertinent
sections of Title 21, Code of Federal Regulations, Chapter I, Subchapter J, are cited in parentheses.
Please consult them before making design or procedural decisions.
Regulatory requirements for radiological products can be found at http://www.fda.gov/RadiationEmittingProducts/default.htm and for medical devices are located at
www.fda.gov/M/devaDvices/default.htm. If you have specific questions about the regulations,
please contact us at: [email protected].
If you have specific questions regarding this software, please contact the eSub team by email at:
[email protected].
Thank you for using our electronic product reporting software. Please communicate your comments
and suggestions to the eSub team as often as you like.
Thank you for your continued support of the FDA Electronic Submission Program (eSub).
An agency may not conduct or sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB control number. The OMB control number for
this information collection is 0910-0025 (expires January 31, 2017).
Role
What is your role?
Information:

!* Manufacturer

The following screen provides several options for you to accurately define what type of
eSubmission you intend to create for FDA. Below are explanations of your options. Please
feel free to review this screen, advance to the next screen and view the picklists, but if you're
confused, come back to read this screen again to be certain you are selecting the correct
report or correspondence type you want to create.

Submission Information
Step 1

Use the radio buttons to identify the type of submission you are preparing.
(Supplements should be prepared using the same document type as the original
submission.)

What Type of Submission is this? (Supplements should be submitted
selecting the same document type as the original report.)

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!* (•) Radiation Safety

Report (Product) Report
(21 CFR 1002.10)
( ) Annual Report (21
CFR 1002.13)
( ) Laser Light Show
Documents (all relevant
documents) (21 CFR
1040.11(c))
( ) Correspondence

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( ) Variance Request
(General, not Laser Light
Show) (21 CFR 1010.4)
( ) Laser Original
Equipment/Component
Manufacturer Registration
(21 CFR 1040.10(a)(3)(ii))
( ) Abbreviated Report
(21 CFR 1002.12)
Step 2

After answering the Submission Type question above, one of the questions below
may become active and required (see the blue dot to the right of the question). If there
is an active question, select the appropriate product area or document type from the
question's pick list.

What Type of Product is this Radiation Safety Report about?

!*

Therapy Ultrasound Products
What Type of Product is this Annual Report about?
What Laser Light Show Document are you filing?
What Type of Correspondence is this?
What Type of Product is this Variance Request about?

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Manufacturer Data
Manufacturer Responsible for Product Compliance
Note:

This is the firm that takes responsibility for certification that the product meets the
performance standard. This firm develops and maintains the quality control and testing
program that is the basis for the certification of this product. Additionally, this firm usually is
the owner of the product design and manufacturing process design.
Be sure to enter address information for each tab below:

Select the Manufacturer's address from the Establishment Address book:

*

Establishment Information:
Establishment Name
Division Name
Home Page
Physical Location:
Address
Telephone Number
Fax Number
Mailing Location:
Address
Telephone Number
Fax Number

Responsible Individual
Note:

The responsible individual is the highest level and most responsible individual affiliated with
this establishment.

Select the Responsible Individual from the Contact Address book:

*

Contact Information:
Contact Name
Occupation Title
Email Address
Establishment Information:
Establishment Name
Division Name
Physical Location:
Address
Telephone Number
Fax Number

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Mailing Location:
Address
Telephone Number
Fax Number

Manufacturer's Reporting Official
Note:

This is the person at the manufacturing facility that is knowledgeable and responsible for
addressing all aspects of the testing and quality control procedures for certification as
reported to FDA in the product report. Documentation of changes intesting and quality
control procedures submitted to FDA must be signed by this individual.

Select the Reporting Official from Contact Address book:

*

Contact Information:
Contact Name
Occupation Title
Email Address
Establishment Information:
Establishment Name
Division Name
Physical Location:
Address
Telephone Number
Fax Number
Mailing Location:
Address
Telephone Number
Fax Number

Report Submitter
Note:

The submitter may be a consulting individual or firm providing assistance in report
preparation and maintenance. Documents or submissions such as this one that are prepared
by the submitter must have an accompanying authorization letter from the manufacturer's
reporting official for authenticity.

Select the Submitter from the Contact Address book:

*

Contact Information:
Contact Name
Occupation Title
Email Address
Establishment Information:
Establishment Name
Division Name

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Physical Location:
Address
Telephone Number
Fax Number
Mailing Location:
Address
Telephone Number
Fax Number
Comments:
Internal Reference Number:

Parent Establishment
Is there a parent establishment?

*

Select the Parent Establishment and Contact from the Contact Address book:
Contact Information:
Contact Name
Occupation Title
Email Address
Establishment Information:
Establishment Name
Division Name
Physical Location:
Address
Telephone Number
Fax Number
Mailing Location:
Address
Telephone Number
Fax Number

Manufacturer Designated United States Agent
Note:

Manufacturers exporting to the U.S. must designate a U.S. agent, see 21 CFR 1005.25.

Is there a United States agent that has been designated by the manufacturer?

*

Importer

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Additional Manufacturing Locations

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Product Data
Product and Model Identification

Attention - Information about this section
In this section you'll be asked to identify several required or optional things which will help
FDA/CDRH staff to prioritize their reviews. You'll be asked to consider the following aspects:
(1) Identify your product's radiation type and the CDRH Product Code.
(2) Enter an Accession number if this will be a report supplment. If you are preparing a supplement,
you'll see that after entering a valid 7-digit Accession number many questions will no longer be
required (they will either be disabled or will be optional, meaning they will no longer have the blue
dot).
(3) You will also have several questions that are of high significance for FDA/CDRH - why you
might be submitting this report or correspondence. Please read these questions carefully, referring to
the 21 CFR regulations on the website www.FDA.gov if you are unsure if the question is relevant to
your firm's situation.
(4) If you find that you have more information that you want the FDA/CDRH to read but it doesn't
seem to fit under other questions, we have a final "Additional Information" question in this section
which invites you to add comments and/or attach a file that provides further information from your
firm about this submission. This is the place to add that extra information.

Product Type Reported
What is the product code?

*

To select the three letter product code,
- Click the plus sign. You will see a product code filter dialog box.
- Select the appropriate category name from the pick list. You will be provided a list of product codes
from which to choose.
- Select the best match to your product.
- The remaining fields will be filled in for you when you select your product code.
Category
Product Code
Performance
Standard
If Other, provide a category name for this specific product.

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Report Information
Is this the first time you've submitted a report on the particular type of product selected
in the Product Type Reported section?

*

Since this is not the first time you've reported on this type of product, then is this a report
supplement to a previously reported model family?
Provide the Accession Number of the original report for which this is a supplement:
(Note: Do not enter any Device Premarket Application or Notification document number here,
such as PMAs, 510(k)s, IDEs, etc. See Accession number description below.)
Are you requesting a new variance, a renewal, extension or amendment to a
previous variance?
Stop:

*

If you are requesting a new variance, renewal, extension, or amendment, you must file a
Variance Request separate from this report. To do this, open a new report (File > New) and
select either "Laser Light Show Variance Request" or "Variance Request (General, not Laser
Light Show)" as your Type of Submission in the Submission Information Screen. If you select
"Variance Request (General, not Laser Light Show)r" you must select the product for which
you are requesting a variance with the pick list in the bottom section of the screen.

Special Considerations

Information:

If this product will require a formally approved Variance from a certain performance
requirement, you will need to complete two Reports for FDA, both (1) this Radiation Safety
Report (RSR) on this product, and (2) a Variance Request report. This eSubmitter software
application package includes a general Variance Request form as well as the specific Laser
Light Show Variance Request form. Both the Product RSR file and the appropriate Variance
Request Correspondence file must be submitted to CDRH following the regular files
packaging procedures in this application. Both may be transferred to the same CD or
submitted via the FDA ESG to submit to the FDA/CDRH.
In addition, any Variance Request form must be printed out and the signed hard-copy sent to
FDA's Division of Dockets Management at:
Division of Dockets Management (HFA-305)
Food and Drug Administration
5630 Fishers Lane
Rockville, MD 20852
NOTE: There is no need to send a copy of the CD to Division of Dockets Management.

Noncompliances or Defects
Does this document or any of its attachments contain:
A notification of noncompliance or defect?

*

You may provide an explanation and/or attach a document here:
Details

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Responses to Noncompliances or Defects
Does this document or any of its attachments contain any of these responses concerning
noncompliances or defects?
A refutation of noncompliances or defects identified to your firm?

*

A request for an exemption from notification to purchasers (see 21 CFR 1003.21 and 1003.30)?

*

Corrective action plans you intend to implement to correct noncompliances or defects discovered in
past or current production?

*

Note:

If you are submitting a Corrective Action Plan (CAP) following 21 CFR 1004 and information
on design changes for future production, the design change information must be submitted in
a Radiation Safety (Product) Report or supplemental report. Both the proposed CAP and the
design changes may be submitted in one document if you prepare a product report and
choose to include the CAP in it as a file attachment. Alternatively, you may create a separate
eSubmission for the CAP using the "Correspondence" type template and selecting "Followup correspondence to FDA."

A description of any design changes that correct noncompliances for future production?
Note:

*

If you are submitting information on product design changes for future production due to a
discovery of noncompliances or defects in current production, you must use the Radiation
Safety (Product) Report template to create the report . Correspondence templates may be
used to submit other information such as a proposed corrective action plan pertaining to a
noncompliance or defect.

You may add an explanation and/or attach a document here:
Details

Exemption Requests
Does this document or any of its attachments contain:
Exemption of a product for government use from a standard (21 CFR 1010.5)?

*

Exemption for products for government use from reporting and recordkeeping (21 CFR 1002.51)?

*

Special exemption of products from reporting and/or recordkeeping (21 CFR 1002.50)?

*

Request for approval of alternate labeling?

*

Application for alternate test procedures (21 CFR 1010.13)?

*

You may provide an explanation and/or attach any relevant documents here:

Variance Requests
Information:

Please note: in addition to responding to these questions below, a separate General
Variance Request or Laser Light Show Variance Request form must be completed and
submitted to CDRH, with a hard copy sent to FDA's Division of Dockets Management as
instructed below for any variance request. The information requested on this screen does not
constitute the full structured content of the variance request. The 2 types of Variance forms
can be created in eSubmitter by selecting the appropriate Variance submission type under
the eRad Health Menu section of this application.

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Message:

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Click the plus sign to list the requirements from which you are requesting a variance.

This submission includes an application for a variance from certain requirements.
Item

No Information Provided.

Provide an explanation and attach supporting files, if necessary. Click on the plus sign below to attach files.
Details
Stop:

For all Variance requests, two submissions must be made to the FDA.
The electronic version should be submitted following the Packaging Files for Submission
instructions located under Output in the Menu bar, and explained in subsection 4.3 of the
User Manual. If sending a CD & submittal letter, please mail to:
U.S. Food and Drug Administration
Center for Devices and Radiological Health
Attn: eSubmitter Team
Document Mail Center - WO66-0609
10903 New Hampshire Avenue
Silver Spring, MD 20993-0002
Additionally, a paper version (hard-copy) of the signed Variance request document should be
submitted to:
Food and Drug Administration
Division of Dockets Management (HFA-305)
5630 Fishers Lane, Room 1061
Rockville, MD 20857

Responses to Communications from FDA
Does this document or any of its attachments contain:
A response to an FDA inspection?

*

What was the date of the inspection?
A response to a Warning letter or a Notification of Noncompliance or Defect from the
FDA?

*

What was the date of the Warning Letter or other notification letter?
A response to a report review inquiry from the CDRH (the inquiry may have been in the
form of a letter, email, or phone call)?

*

What was the date of the inquiry?
A response to any other communication from FDA?

*

What was the date of the communication?
Provide an explanation:

Additional Information
Here's your opportunity to add anything else to this submission that you want to tell the FDA!

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Is there any other relevant information or additional comments that would help expedite the review of this
submission? Click the plus sign below to attach any supporting files.
Details

Private Labeling
Is the product sold by other companies under different brand names?

*

Medical Devices
Provide the premarket 510(k), IDE, HDE, PDP, or PMA filing numbers related to this medical product, if one
of these numbers has been assigned by FDA yet.

If it has not been submitted yet, or if your device is exempt from premarket clearance or approval, please
provide an explanation. The device regulations can be found in 21 CFR 807 - device manufacturer
registration and device listing.

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Ultrasonic Therapy Product
Model Designation
Note:

Report the model name and/or number, model family, brand name, or other designation of
the product. If reporting a model family, provide the model designation of each model. If you
do not have a model family or brand name, leave the field blank.

Model Designation (Names and/or Numbers):
Item

Model Name

Family Name

*
Brand Name

Product Classification
Indicate below the type of product or family of products covered by this report.
This report covers:
Is your system a continuous-wave (CW) unit or an amplitude-modulated (AM)
unit?

Performance Specifications
Note:

The information reported in this section will be used to determine whether the product
complies with the requirements set forth in 21 CFR 1050.10(c). Several items must be
reported in terms of definitions that are provided by the standard; please refer to 21 CFR
Part 1050.10 for these definitions.

Frequency of Operation
Note:

Provide the following data for operating frequency(ies) in MHz for either fixed, variable, or
multiple frequency systems.

Fixed at _____ MHz:
_____ MHz:
Variable, from _____ MHz to _____ MHz:
Minimum MHz:
Maximum MHz:
Multiple, fixed at _____ MHz, _____ MHz, and _____ MHz:
_____ MHz:
_____ MHz:
_____ MHz:
Operating frequency (ies) are indicated to the user by:

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Output Parameters for Continuous-Wave Units
Temporal-average ultrasonic power:
Message:

Variable, from _____ Watts to _____ Watts:

Minimum Watts:
Maximum Watts:
Indicated to the user by:
Temporal-average effective intensity:
Message:

Variable, from _____ W/cm² to _____ W/cm²:

Minimum W/cm²:
Maximum W/cm²:
Indicated to the user by:

Output Parameters for Amplitude-Modulated Units
Temporal-maximum ultrasonic power:
Message:

Variable, from _____ Watts to _____ Watts:

Minimum Watts:
Maximum Watts:
Indicated to the user by:
Temporal-maximum effective intensity:
Message:

Variable, from _____ W/cm² to _____ W/cm²:

Minimum W/cm²:
Maximum W/cm²:
Indicated to the user by:
Output pulse width:
Message:

Fixed at _____ milliseconds:

_____ milliseconds:
Message:

Variable from _____ milliseconds to _____ milliseconds:

Minimum milliseconds:
Maximum milliseconds:
Indicated to the user by:
Output pulse repetition rate:
Message:

Fixed at _____ pulses/second:

_____ pulses/second:
Message:

Variable, from ______ to ______ pulses/second:

Minimum pulses/second:
Maximum pulses/second:

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Message:

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User selected from the available settings (list available settings):

Setting 1:
Setting 2:
Setting 3:
Indicated to the user by:

Timer Specifications
Timer accuracy for settings of:
Less than 5 minutes:
Provide the number of minutes: (+/- ______ minutes)
Between 5 and 10 minutes:
Provide the number of minutes as a percent: (+/- ______ percent)
Greater than 10 minutes:
Provide the number of minutes: (+/- ______ minutes)
Maximum timer setting: ( ____ minutes)
How does ultrasonic emission automatically terminate at the end of preset time?
How can ultrasonic emission be terminated prior to the end of the preset time?
How is radiation emission routinely terminated?

Applicators
Type of applicators:
Collimating, with an effective radiating area (ERA) of _____ cm²:
Diverging, with an effective radiating area (ERA) of _____ cm²:
Focusing, with focal area of _____ cm² and a focal length of _____ cm:
Transducer Configuration:
Single Crystal (specify material):
For multiple elements, describe each element, the manner in which connected, and the resulting effect on the
radiated field.

Cables
How is application of electrical power to the transducer indicated to the user?

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How is a broken cable or open connection indicated to the user?

Labeling Requirements
Note:

The information reported in this section will be used to determine whether the product
complies with the requirements set forth in 21 CFR Parts 801, 1010.2, 1010.3 and 1050.10
(d). Most of the items below require that a copy of the label be attached; if labels are
unavailable at the time of reporting, please provide a specification control drawing.

Certification
Note:

Part 1010.2 of 21 CFR requires that the product (generator and applicator, if detachable)
bear a permanently affixed tag or label certifying that it complies with the provisions of Part
1050.10. Provide the following information concerning the certification label:

The manner in which the label is attached:
The location of the label:
Attach a sample of the label.
Details

Identification
Note:

Part 1010.3 of 21 CFR requires that the product (generator and applicator, if detachable)
bear a permanently affixed tag or label giving the following information:(a) The name and
address of the manufacturer. (Where the product is sold under a name other than that of the
manufacturer, the name and address of the individual or company under whose name the
product is sold may be given on the label, provided that such individual or company has
previously supplied the CDRH with the name and address of the manufacturer.)(b) The
place, month, and year of manufacture. (The place of manufacture may appear in coded
form if the manufacturer has previously supplied the CDRH with the codes and their
meaning). The month and year of manufacture must be given without abbreviation and with
the year as a four-digit number (for example: Manufactured: September 1978.)

Message:

Provide the following information concerning the identification label:

The manner in which the label is attached:
The location of the label:
Attach a sample of the label.
Details

Generator Labels

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Note:

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Part 1050.10(d)(3) of 21 CFR requires that each ultrasonic therapy generator bear a label
giving the following information:
(a) The brand name, model designation, and serial number of the generator.
(b) The ultrasonic frequency (unless variable, and indicated on the controls).
(c) The type of waveform (continuous wave or amplitude modulated).
In addition to the above, generators employing amplitude modulated waveforms are required
to bear additional labeling giving the following information:
(a) Pulse duration and repetition rate (unless variable, and indicated on the controls).
(b) An illustration of the waveform.
(c) The ratio of the temporal-maximum effective intensity to the temporal-average effective
intensity. If this ratio is a function of any operation control setting, then the range of the ratio
shall be given, and the waveform illustration shall be for the maximum value of this ratio.

Message:

Provide the following information concerning the generator label:

The manner in which the label is attached:
The location of the label:
Attach a sample of the label.
Details

Applicator Labels
Note:

Part 1050.10(d)(4) of 21 CFR requires that each ultrasonic therapy applicator bear a label
giving the following information:(a) The brand name, model designation, and serial number of
the applicator.(b) Thedesignation of the generator for which the applicator is intended.(c) The
ultrasonic frequency, effective radiating area, maximum beam nonuniformity ratio, type of
applicator (focusing, collimating, diverging), and, for focusing applicators, the focal length
and focal area.

Message:

Provide the following information concerning the applicator label:

The manner in which the label is attached:
Attach a sample of the label.
Details

Operation Controls
Note:

Part 1050.10(d)(1) of 21 CFR requires that each operation control be clearly labeled,
identifying the function controlled and, where appropriate, the units of measure of that
function. If a separate control and indicator are associated with the same function, labeling
the units of measure of that function is required for the indicator but not for the control.

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Provide drawings, photographs, or other documents, which show clearly the location and labeling of all such
controls. Click on the Add... button below to attach and select the files.
Details

Service Controls
Note:

Part 1050.10(d)(2) of 21 CFR requires that each service control that is accessible without
displacement or removal of any part of the product be clearly labeled, identifying the function
controlled and including the phrase for service adjustment only.

Provide drawings, photographs, or other documents, which show clearly the location and labeling of all such
controls. Click on the Add... button below to attach and select the files.
Details

Information Requirements
Note:

Provide the following information regarding servicing information, user information, and
product description.

Servicing Information
Note:

Part 1050.10(f) (1) of 21 CFR requires a manufacturer to provide to servicing dealers and
distributors adequate instructions for operation, service, and calibration of the product. This
must include:(a) A description of those controls and procedures that could be used to
increase radiation emission levels.(b) A schedule of maintenance necessary to keep the
product in compliance with 21 CFR 1050.10.(c) Any safety precautions that may be
necessary regarding ultrasonic exposure.

Attach a copy of the servicing information clearly identified above. Click on the Add... button below to attach
and select the files.
Details

User Information
Note:

Part 1050.10(f)(2) of 21 CFR requires a manufacturer to provide users with adequate
instructions for assembly, operation, and safe use of the product. This must include:
(a) A discussion of all operation controls and a description of the effect of each control.
(b) A schedule of maintenance necessary to keep the product in compliance with 21 CFR
1050.10.
(c) Any safety precautions that may be necessary regarding ultrasound exposure.
(d) A description (including textual discussion and diagrams, plots or photographs) of the
spatial distribution of the radiated field. The description must include the statement that it
applies for the radiation emitted into the equivalent of an infinite medium of distilled,
degassed water at 30°C and with line voltage variations in the range of ± 10%, or the rated
value.
(e) The uncertainties in magnitude, expressed in percentage error, of the ultrasonic

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frequency, effective radiating area, and (when applicable) the ratio of the temporal-maximum
to temporal-average effective intensity, pulse duration, pulse repetition rate, focal area, and
focal length.
(f) The error in indication of radiated power and intensity.
(g) The error in indication of present treatment time.
(h) A listing of all controls, adjustments, and procedures for operation and maintenance,
including the warning "Caution -- use of controls or adjustments or performance of
procedures other than those specified herein may result in hazardous exposure to ultrasonic
energy."
Attach a copy of the user information to the preceding sections, clearly identified above. Click on the Add...
button below to attach and select the files.
Details

Product Description
Note:

In order to adequately review a manufacturer's product, CDRH requires that a product report
provide a thorough physical description of the product. Such a description must include:(a)
Photographs or drawings or the generator and applicator.(b) A complete schematic diagram
of the product.

Provide the information listed above as attachments. Click on the Add... button below to attach and select the
files.
Details

Testing Programs
Note:

The information reported in this section will be used to determine whether the manufacturer's
testing programs are adequate for certification (21 CFR 1010.2) and that the products are in
compliance with the performance standard. Each item in this section must be addressed
individually and in detail.

Incoming Component Testing
Note:

Fully describe all tests that are performed on components whose perfomance can affect
compliance with this standard. This description should include but is not limited to:(a) Identify
the component tested and its function.(b) State whether the component is tested on a 100
percent or sampling basis. If tested on a sampling basis, provide all sampling parameters
and the basis for selecting the Acceptable Quality Level.(c) Describe the corrective action
taken following unit or lot rejection (i.e., return component to manufacturer, test 100 percent
of components, increasesampling level). If the sampling level is increased, provide the
complete rationale for this procedure, and any revised acceptance criteria.

Provide the above information as an attachment for each tested component. For example, if transducer
crystals and timers are among the components tested, attach the description of the testing of crystals as one
file attachment and the description of the testing of timers as the second file attachment, and so forth. Click
on the Add... button to add and select the files to be attached.
Details

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Calibration of Test Instruments
Note:

Fully describe the instruments used in any test conducted to ensure compliance with this
standard. This should include, but is not limited to, the following:(a) The manufacturer, model
number, type (e.g., radiation force), accuracy, and resolution of the instrument used to
measure ultrasonic power.(b) The procedure by which the above instrument is calibrated.
Include a description of any calibrated source used, stating the accuracy and by whom
calibrated.(c) The manufacturer, model number, and complete specifications of the
hydrophone used to measure ultrasonic intensity.(d) A description of the scanning apparatus
used to measure the spatial distribution of the radiated field.(e) A description of, and
calibration procedures for, any other instrument used for compliance testing.

Provide the above information as attachments below. Click on the Add... button to add and select the files to
be attached.
Details

Production Testing
Note:

Fully describe all tests that are performed on the product during or after production to ensure
compliance with this standard. The description of each test must include, but is not limited to,
items (a) through (e) below. Note that part 1050.10(e) of 21 CFR requires that
measurements of ultrasonic radiation be made with the radiation emitted into the equivalent
of an infinite medium of distilled, degassed water at 30°C, and with line voltage variations in
the range of ±10% of the rated value.
(a) Identify all instruments reported in the Calibration of Test Instruments section above that
are used for the test.
(b) State the sources and magnitudes of uncertainty in the test.
(c) State whether the component or parameter is tested 100 percent or sampling basis. If
tested on a sampling basis, include lot size, proportion of total production tested, method of
sample selection to ensure randomness, and the rationale for sampling rather than testing on
a 100 percent basis. It must be clearly demonstrated that such a sampling program will
ensure compliance of all certified products.
(d) Decribe the test procedure in detail, including any assumptions that are taken from the
results. For example, in the description of the test for accuracy of indicated power, state the
specific power levels at which the measurement is made, the error in indicated power at
each point, and the range over which the average error is assumed to hold.
(e) Describe the corrective action taken following unit or lot rejection (i.e., Increase sampling,
test 100 percent).

Provide the above information as an attachment for each parameter tested. For example, present the
description of the test for error in indicated power as a file attachment. Click on the Add... button to add and
select the files to be attached. The parameters tested during production should include, but are not limited to:
(a) Error in indication of temporal-average ultrasonic power (CW units).
(b) Error in indication of temporal-maximum ultrasonic power (pulsed units).
(c) Error in measured value of effective radiating area.
(d) Error in the determination of the ratio of temporal-maximum effective intensity to temporal-average
effective intensity.

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(e) Error in indication of preset treatment time.
(f) Proper operation of manual and automatic treatment termination devices.(g) Proper operation of visual
"ultrasound on" indicator.
(h) Proper operation of indicators of pulse duration, pulse repetition rate, and ultrasonic frequency (where
applicable).
Details

Life Testing
Note:

Fully describe all tests that are performed on the product to ensure that it is capable of
complying with the standard throughout its life. This should include, but is not limited to:(a)
Sample size, frequency of sampling, and selection criteria.(b) Description of the test,
including the sources and magnitudes of error, parameters measured or monitored,
instruments used, and length of test or equivalent length of test.

Provide the above information as an attachment. Click on the Add... button below to add and select the files
to be attached.
Details
Provide an estimate of the useful life of the product (in years):
Stop:

You have reached the end of this report. Please verify that all PDFs that are to be included in
this submission are correctly attached to a specific file attachment question. Otherwise, they
will not be packaged with your report. Check to make sure you have no missing data (select
Missing Data Report from the Output menu). Once you have confirmed that there is no
missing data and all your files are attached, click on the Package Submission icon on the
tool bar.

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