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Title 21 published on 2015-04-01.
No entries appear in the Federal Register after this date, for 21 CFR Part 1010.
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.
§ 351 - Adulterated drugs and devices
§ 352 - Misbranded drugs and devices
§ 360 - Registration of producers of drugs or devices
§ 360e - Premarket approval
21 U.S. Code § 221 to 237 - Repealed. July 1, 1944, ch. 373, title XIII,
§ 360f - Banned devices
§ 360g - Judicial review
§ 360h - Notification and other remedies
§ 360i - Records and reports on devices
§ 360j - General provisions respecting control of devices intended for human use
§ 360hh - Definitions
§ 360ii - Program of control
§ 360jj - Studies by Secretary
§ 360kk - Performance standards for electronic products
21 U.S. Code § -
§ 360mm - Imports
§ 360nn - Inspection, records, and reports
§ 360pp - Enforcement
§ 360qq - Repealed.
§ 360rr - Federal-State cooperation
§ 360ss - State standards
§ 371 - Regulations and hearings
§ 381 - Imports and exports