03-55524. Ophthalmic Devices  

  • Start Preamble

    CFR Correction

    In Title 21 of the Code of Federal Regulations, Parts 800 to 1299, revised as of April 1, 2003, in § 886.1500, on page 456, paragraph (b) is added to read as follows:

    Headband mirror.
    * * * * *

    (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 § 886.9. The device is also exempt from the current good manufacturing practice regulations in part 820 of this chapter, with the exception of § 820.180, with respect to general requirements concerning records, and § 820.198, with respect to complaint files.

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    [FR Doc. 03-55524 Filed 8-15-03; 8:45 am]

    BILLING CODE 1505-01-D

Document Information

Published:
08/18/2003
Department:
Food and Drug Administration
Entry Type:
Rule
Document Number:
03-55524
Pages:
49351-49351 (1 pages)
PDF File:
03-55524.pdf