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.
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.