PREMARKET APPROVAL OF MEDICAL DEVICES

ICR 199004-0910-004

OMB: 0910-0231

Federal Form Document

Forms and Documents
Document
Name
Status
No forms / supporting documents in this ICR. Check IC Document Collections.
IC Document Collections
IC ID
Document
Title
Status
109908
Migrated
ICR Details
0910-0231 199004-0910-004
Historical Active 198906-0910-010
HHS/FDA
PREMARKET APPROVAL OF MEDICAL DEVICES
Reinstatement with change of a previously approved collection   No
Regular
Approved without change 07/11/1990
Retrieve Notice of Action (NOA) 04/13/1990
  Inventory as of this Action Requested Previously Approved
06/30/1993 06/30/1993
800 0 0
536,000 0 0
0 0 0

THIS RULE DESCRIBES THE CONTENTS OF A PREMARKET APPROVAL APPLICATION (PMA) FOR A MEDICAL DEVICE. THE FDA REQUIRES THIS INFORMATION FROM MEDICAL DEVICE MANUFACTURERS IN ORDER TO GET APPROVAL FOR MARKETING DEVICES SHOWN TO BE SAFE AND EFFECTIVE, OR DISAPPROVE DEVICES NOT SHOWN TO BE SO.

None
None


No

1
IC Title Form No. Form Name
PREMARKET APPROVAL OF MEDICAL DEVICES

  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 800 0 0 0 800 0
Annual Time Burden (Hours) 536,000 0 0 0 536,000 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No

$0
No
No
Uncollected
Uncollected
Uncollected
Uncollected

  No

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:
 
 
 
 
 
 
 
    (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;
 
 
 
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.
04/13/1990


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