
[Federal Register: May 5, 2010 (Volume 75, Number 86)]
[Notices]               
[Page 24707]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr05my10-96]                         

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2009-N-0486]

 
Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approval; Guidance for Industry, Food and Drug 
Administration, and Foreign Governments: Fiscal Year 2010 Medical 
Device User Fee Small Business Qualification and Certification

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 ``Guidance for Industry, FDA, and 
Foreign Governments: Fiscal Year 2010 Medical Device User Fee Small 
Business Qualification and Certification'' has been approved by the 
Office of Management and Budget (OMB) under the Paperwork Reduction Act 
of 1995.

FOR FURTHER INFORMATION CONTACT: Daniel Gittleson, Office of 
Information Management, Food and Drug Administration, 1350 Piccard Dr., 
PI50-400B, Rockville, MD 20850, 301-796-5156, 
Daniel.Gittleson@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: In the Federal Register of January 19, 2010 
(75 FR 2874), 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 0910-0508. 
The approval expires on February 28, 2013. A copy of the supporting 
statement for this information collection is available on the Internet 
at http://www.reginfo.gov/public/do/PRAMain.

    Dated: April 29, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-10581 Filed 5-4-10; 8:45 am]
BILLING CODE 4160-01-S

