[Federal Register Volume 64, Number 44 (Monday, March 8, 1999)]
[Notices]
[Page 11018]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-5518]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration
[Docket No. 98N-0453]


Agency Information Collection Activities; Announcement of OMB 
Approval; Medical Devices: Third-Party Review Program Under the U.S./EC 
MRA

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 Devices: Third-Party 
Review Program Under the U.S./EC MRA'' has been approved by the Office 
of Management and Budget (OMB) under the Paperwork Reduction Act of 
1995.

FOR FURTHER INFORMATION CONTACT: Peggy Schlosburg, 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 December 14, 1998 
(63 FR 68773), 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 0910-0378. 
The approval expires on February 28, 2002. A copy of the supporting 
statement for this information collection is available on the Internet 
at ``http://www.fda.gov/ohrms/dockets''.

    Dated: March 1, 1999.
William K. Hubbard,
Acting Deputy Commissioner for Policy.
[FR Doc. 99-5518 Filed 3-5-99; 8:45 am]
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