[Federal Register Volume 68, Number 76 (Monday, April 21, 2003)]
[Notices]
[Page 19547]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 03-9810]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 02N-0405]


Agency Information Collection Activities; Announcement of OMB 
Approval; Medical Device Reporting: Manufacturer Reporting, Importer 
Reporting, User Facility Reporting, and Distributor Reporting

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Medical Device Reporting: 
Manufacturer Reporting, Importer Reporting, User Facility Reporting, 
and Distributor Reporting'' has been approved by the Office of 
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Peggy Robbins, Office of Information 
Resources Management (HFA-250), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857, 301-827-1223.

SUPPLEMENTARY INFORMATION: In the Federal Register of January 9, 2003 
(68 FR 1187), the agency announced that the proposed information 
collection had been submitted to OMB for review and clearance under 44 
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not 
required to respond to, a collection of information unless it displays 
a currently valid OMB control number. OMB has now approved the 
information collection and has assigned OMB control number 0910-0437. 
The approval expires on April 30, 2006. A copy of the supporting 
statement for this information collection is available on the Internet 
at http://www.fda.gov/ohrms/dockets.

    Dated: April 14, 2003.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 03-9810 Filed 4-18-03; 8:45 am]
BILLING CODE 4160-01-S