BUREAU OF MEDICAL DEVICES STANDARDS SURVEY

ICR 198301-0910-007

OMB: 0910-0115

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
109617 Migrated
ICR Details
0910-0115 198301-0910-007
Historical Inactive 198012-0910-001
HHS/FDA
BUREAU OF MEDICAL DEVICES STANDARDS SURVEY
Extension without change of a currently approved collection   No
Regular
Disapproved 03/11/1983
Retrieve Notice of Action (NOA) 01/17/1983
NOT APPROVED. FDA HAS NOT PROVIDED A COMPELLING ARGUMENT THAT THIS INFORMATION COLLECTION IS NECESSARY ON AN ANNUAL BASIS. FDA SHOULD RESUBMIT THIS REQUEST IN 1984 FOR APPROVAL.
  Inventory as of this Action Requested Previously Approved
03/11/1983 01/31/1983
0 0 37
0 0 74
0 0 0

THE PURPOSE OF THE BUREAU OF MEDICAL DEVICES STANDARDS SURVEY IS TO PROVIDE A COMPREHENSIVE LISTING OF CURRENT NATIONAL AND INTERNATIONAL STANDARDS PROMULGATION ACTIVITIES IN THE FIELD OF MEDICAL DEVICES.

None
None


No

1
IC Title Form No. Form Name
BUREAU OF MEDICAL DEVICES STANDARDS SURVEY FDA 3196

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.
01/17/1983


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