[Federal Register Volume 76, Number 98 (Friday, May 20, 2011)]
[Rules and Regulations]
[Page 29153]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2011-12410]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 878

[Docket No. FDA-2006-N-0045; Formerly Docket No. 2006N-0109]


Medical Devices; Reclassification of the Topical Oxygen Chamber 
for Extremities; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a final 
rule that appeared in the Federal Register of April 25, 2011 (76 FR 
22805). The document announced that FDA is reclassifying the topical 
oxygen chamber for extremities (TOCE) from class III to class II. The 
document published inadvertently used outdated contact information. 
This document corrects that error.

DATES: Effective May 25, 2011.

FOR FURTHER INFORMATION CONTACT: Charles N. Durfor, Center for Devices 
and Radiological Health, Food and Drug Administration, 10903 New 
Hampshire Ave., Bldg. 66, Rm. G424, Silver Spring, MD 20993-0002, 301-
796-6438.

SUPPLEMENTARY INFORMATION: In FR Doc. 2011-9899 appearing on page 22805 
in the Federal Register of Monday, April 25, 2011, the following 
correction is made: 1. On page 22805, in the third column, the FOR 
FURTHER INFORMATION CONTACT section is corrected to read as follows:

FOR FURTHER INFORMATION CONTACT: Charles N. Durfor, Center for 
Devices and Radiological Health, Food and Drug Administration, Bldg. 
66, Rm. G424, 10903 New Hampshire Ave., Silver Spring, MD 20993-
0002, 301-796-6438.

    Dated: May 17, 2011.
 Nancy K. Stade,
Deputy Director for Policy, Center for Devices and Radiological Health.
[FR Doc. 2011-12410 Filed 5-19-11; 8:45 am]
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