[Federal Register Volume 71, Number 235 (Thursday, December 7, 2006)]
[Notices]
[Page 70973]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E6-20705]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2006N-0426]


Withdrawal of Federal Register Notice

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; withdrawal.

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SUMMARY: The Food and Drug Administration (FDA) is announcing the 
withdrawal of a 60-day notice that published in the Federal Register of 
October 31, 2006 (71 FR 63765). The document published in error.

DATES: December 7, 2006.

FOR FURTHER INFORMATION CONTACT: Denver Presley, Jr., Office of the 
Chief Information Officer (HFA-250), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857, 301-827-1472.

SUPPLEMENTARY INFORMATION: FDA is withdrawing a 60-day notice entitled 
``Medical Device User Fee and Modernization Act Small Business 
Qualification Certification (Form FDA 3602),'' which published in the 
Federal Register of October 31, 2006 (71 FR 63765), because it is a 
duplicate of an earlier 60-day notice. The earlier 60-day notice 
published in the Federal Register of August 29, 2006 (71 FR 51196). The 
October 31 notice was published in error.

    Dated: November 30, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6-20705 Filed 12-6-06; 8:45 am]
BILLING CODE 4160-01-S