MEDICAL DEVICE REPORTING

ICR 198610-0910-009

OMB: 0910-0201

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
165477
Migrated
ICR Details
0910-0201 198610-0910-009
Historical Active 198409-0910-003
HHS/FDA
MEDICAL DEVICE REPORTING
No material or nonsubstantive change to a currently approved collection   No
Emergency 10/08/1986
Approved with change 10/08/1986
Retrieve Notice of Action (NOA) 10/08/1986
  Inventory as of this Action Requested Previously Approved
12/31/1986 12/31/1986
27,660 0 0
109,376 0 0
0 0 0

REQUIRES A MANUFACTURER OR IMPORTER OF MEDICAL DEVICES TO REPORT TO FD WHENEVER THEY POSSESS INFORMATION THAT REASONABLY SUGGESTS THAT A DEVICE HAS CAUSED OR CONTRIBUTED TO A DEATH OR SERIOUS INJURY. IMPORTERS ARE REQUIRED TO ESTABLISH AND MAINTAIN FILES OF REPORTS AND RECORDS.

None
None


No

1
IC Title Form No. Form Name
MEDICAL DEVICE REPORTING

  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 27,660 0 0 0 27,660 0
Annual Time Burden (Hours) 109,376 0 0 0 109,376 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.
10/08/1986


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