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Title 21 published on 2013-04-01
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.
21 U.S. Code § 351 - Adulterated drugs and devices
21 U.S. Code § 352 - Misbranded drugs and devices
21 U.S. Code § 360 - Registration of producers of drugs or devices
21 U.S. Code § 360c - Classification of devices intended for human use
21 U.S. Code § 360d - Performance standards
21 U.S. Code § 360e - Premarket approval
21 U.S. Code § 360h - Notification and other remedies
21 U.S. Code § 360i - Records and reports on devices
21 U.S. Code § 360j - General provisions respecting control of devices intended for human use
21 U.S. Code § -
21 U.S. Code § 371 - Regulations and hearings
21 U.S. Code § 374 - Inspection
21 U.S. Code § 381 - Imports and exports
21 U.S. Code § 383 - Office of International Relations