MEDICAL DEVICES STANDARDS REPORT

ICR 199210-0910-006

OMB: 0910-0219

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
109881
Migrated
ICR Details
0910-0219 199210-0910-006
Historical Active 198905-0910-005
HHS/FDA
MEDICAL DEVICES STANDARDS REPORT
Reinstatement with change of a previously approved collection   No
Regular
Approved without change 01/07/1993
Retrieve Notice of Action (NOA) 10/28/1992
  Inventory as of this Action Requested Previously Approved
11/30/1995 11/30/1995
19 0 0
37 0 0
0 0 0

THE MEDICAL DEVICE STANDARDS ACTIVITIES REPORT IS A COMPREHENSIVE LISTING OF NATIONAL AND INTERNATIONAL STANDARDS ACTIVITIES. IT SERVES AS GUIDELINES FOR THE CONTINUING REVIEW OF EXISTING STANDARDS AND THE DEVELOPMENT OF NEW STANDARDS. IT IS USED BY GOVERNMENT AGENCIES, HOSPITALS, LIBRARIES, INDUSTRY, AND SMALL BUSINESSES.

None
None


No

1
IC Title Form No. Form Name
MEDICAL DEVICES STANDARDS REPORT

  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 19 0 0 19 0 0
Annual Time Burden (Hours) 37 0 0 37 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
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.
10/28/1992


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