MEDICAL DEVICE REPORTING

Forms and Documents

Document	Type	Status	Availability

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Collection	Type	Status	Form
109843	MEDICAL DEVICE REPORTING	Form	Migrated

ICR Details

OMB Control No: 0910-0201	ICR Reference No: 198702-0910-007
Status: Historical Active	Previous ICR Reference No: 198612-0910-002
Agency/Subagency: HHS/FDA	Agency Tracking No:
Title: MEDICAL DEVICE REPORTING
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 04/30/1987
	Date Received in OIRA: 02/04/1987
Terms of Clearance: THIS INFORMATION COLLECTION REQUEST IS APPROVED FOR FIVE MONTHS UNDER THE FOLLOWING CONDITIONS: 1) A NEW REQUEST WILL BE SUBMITTED IN THREE MONTHS THAT RESPONDS TO AL OF THE CONCERNS RAISED DURING THE PUBLIC MEETING HELD BY OMB ON MARCH 6, 1986. 2) THE FORM CONTAINED IN THE NEW REQUEST WILL BE REVISED IN RESPONSE T THE COMMENTS MADE BY THE HEALTH INDUSTRY MANUFACTURERS ASSOCIATION IN ITS APRIL 7, 1986 LETTER TO OMB WITH CCs TO FDA. 3) THE NEW REQUEST WILL ALSO IDENTIFY THOSE AREAS IN THE REPORTING REQUIREMENTS THAT SHOULD BE REVISED TO MINIMIZE THE REPORTING BURDEN AND A SCHEDULE FOR INITIATING THE RULEMAKING TO IMPLEMENT SUCH REVISIONS.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/1987	09/30/1987	04/30/1987
Responses	15,638	0	15,638
Time Burden (Hours)	58,618	0	58,618
Cost Burden (Dollars)	0	0	0

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Abstract: THIS REGULATION REQUIRES A MANUFACTURER OR IMPORTER OF MEDICAL DEVICES TO REPORT TO FDA WHEN THEY POSSESS INFORMATION SUGGESTING A DEVICE HAS CAUSED OR CONTRIBUTED TO A DEATH OR SERIOUS INJURY, OR HAS MALFUNCTIONED AND IS LIKELY TO CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY. IMPORTERS ARE REQUIRED TO ESTABLISH AND MAINTAIN FILE OF REPORTS AND RECORDS.

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
MEDICAL DEVICE REPORTING	FDA 3322

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ICR Summary of Burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	15,638	15,638	0	0	0	0
Annual Time Burden (Hours)	58,618	58,618	0	0	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 02/04/1987

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