[Federal Register Volume 71, Number 176 (Tuesday, September 12, 2006)]
[Rules and Regulations]
[Page 53569]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 06-55527]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 880


General Hospital and Personal Use Devices

CFR Correction

    In Title 21 of the Code of Federal Regulations, parts 800 to 1299, 
revised as of April 1, 2006, on page 410, in Sec.  880.5950, paragraph 
(b) is corrected to read as follows:


Sec.  880.5950  Umbilical occlusion device.

* * * * *
    (b) Classification. Class I (general controls). The device is 
exempt from the premarket notification procedures in subpart E of part 
807 of this chapter, subject to the limitations in Sec.  880.9.
[FR Doc. 06-55527 Filed 9-11-06; 8:45 am]
BILLING CODE 1505-01-D