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General Hospital and Personal Use Devices

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Information about this document as published in the Federal Register.

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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 § 880.5950, paragraph (b) is corrected to read as follows:

Umbilical occlusion device.
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(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 § 880.9.

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[FR Doc. 06-55527 Filed 9-11-06; 8:45 am]