
[Federal Register Volume 75, Number 234 (Tuesday, December 7, 2010)]
[Notices]
[Pages 76015-76016]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-30679]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2010-N-0551]


Compliance Policy Guide Sec. 393.200 Laser(s) as Medical Devices 
for Facelift, Wrinkle Removal, Acupuncture, Auricular Stimulation, 
Etc.; Withdrawal of Guidance

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 Compliance Policy Guide Sec. 393.200 Laser(s) as Medical 
Devices for Facelift, Wrinkle Removal, Acupuncture, Auricular 
Stimulation, etc. (CPG Sec. 393.200). CPG Sec. 393.200 is included in 
FDA's Compliance Policy Guides Manual, which was listed in the Annual 
Comprehensive List of Guidance Documents that published on August 9, 
2010.

DATES: The withdrawal is effective December 7, 2010.

[[Page 76016]]


FOR FURTHER INFORMATION CONTACT: Sean M. Boyd, Center for Devices and 
Radiological Health, Office of Communication, Education, and 
Radiological Programs, Food and Drug Administration, 10903 New 
Hampshire Ave., Bldg. 66, rm. 4640, Silver Spring, MD 20993-0002, 301-
796-5895.

SUPPLEMENTARY INFORMATION: In a notice containing a cumulative list of 
guidances available from the Agency that published in the Federal 
Register of August 9, 2010 (75 FR 48180 at 48233), FDA included the 
Compliance Policy Guides Manual, which includes CPG Sec. 393.200. FDA 
is withdrawing CPG Sec. 393.200 because it is obsolete.

    Dated: November 23, 2010.
Dara Corrigan,
Associate Commissioner for Regulatory Affairs.
[FR Doc. 2010-30679 Filed 12-6-10; 8:45 am]
BILLING CODE 4160-01-P


