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§807.22. Times for establishment registration and device listing. — Inbound Citations

21 C.F.R. § 807.22

Cited by 7 regulations in release Current.

Citations to 21 C.F.R. § 807.22 as a whole

  • (a) For initial registration and listing, owners or operators who have been granted a waiver from electronic filing using the procedures set forth in § 807.21(b) must send a letter containing all of the registration and listing information described in §§ 807.22, 807.25 (and § 807.26 when such information is requested by FDA), at the times described in § 807.22, to: The Imports and Registration and Listing Team, Division of Regulatory Programs 2, Office of Regulatory Programs, Office of Product Evaluation and Quality, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 1432, Silver Spring, MD 20993-0002.

Citations to §807.22(a)

  • (1) Initial establishment registration information as required by §§ 807.22(a) and 807.25;
  • (c) Failure to submit any of the required information on time, as specified in § 807.22(a) and (b), will put the establishment in a “failed to register” or “failed to list” status as applicable.
    The establishment will not be considered active and the establishment registration and device listing information may not appear on the FDA Web site until the required information is submitted to and processed by FDA.

Citations to §807.22(b)

  • (2) Updates to registration information as required by §§ 807.22(b) and 807.25;
  • (c) Failure to submit any of the required information on time, as specified in § 807.22(a) and (b), will put the establishment in a “failed to register” or “failed to list” status as applicable.
    The establishment will not be considered active and the establishment registration and device listing information may not appear on the FDA Web site until the required information is submitted to and processed by FDA.

Citations to §807.22(b)(1)

Citations to §807.22(b)(3)