21 C.F.R. · Food and Drugs
21 C.F.R. § 822.9

What must I include in my submission?

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 822.9 — What must I include in my submission?

§ 822.9 What must I include in my submission? Your submission must include the following: (a) Organizational/administrative information: (1) Your name and address; (2) Generic and trade names of your device; (3) Name and address of the contact person for the submission; (4) Premarket application/submission number and device identifiers for your device; (5) Table of contents identifying the page numbers for each section of the submission; (6) Description of the device (this may be incorporated by reference to the appropriate premarket application/submission); (7) Product codes and a list of all relevant model numbers; and (8) Indications for use and claims for the device; (b) Postmarket surveillance plan; (c) Designated person information; (1) Name, address, and telephone number; and (2) Experience and qualifications. [67 FR 38887, June 6, 2002, as amended at 78 FR 58823, Sept. 24, 2013]

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21 C.F.R. § 822.9
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The regulatory text of 21 C.F.R. § 822.9 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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boisestandard.org United States Law CFR Title 21 21 C.F.R. § 822.9