CFR › Title 21 › Chapter I › Subchapter H › Part 803

21 CFR Part 803 - MEDICAL DEVICE REPORTING

Authority:
21 U.S.C. 352, 360, 360i, 360j, 371, 374.
Source:
70 FR 9519, July 13, 2005, unless otherwise noted

Title 21 published on 2014-04-01

no entries appear in the Federal Register after this date.

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.

United States Code
U.S. Code: Title 21 - FOOD AND DRUGS

§ 352 - Misbranded drugs and devices

§ 360 - Registration of producers of drugs or devices

§ 360i - Records and reports on devices

§ 360j - General provisions respecting control of devices intended for human use

§ 371 - Regulations and hearings

§ 374 - Inspection