21 CFR Part 809, Subpart C - Requirements for Manufacturers and Producers
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- § 809.20 — General requirements for manufacturers and producers of in vitro diagnostic products.
- § 809.30 — Restrictions on the sale, distribution and use of analyte specific reagents.
- § 809.40 — Restrictions on the sale, distribution, and use of OTC test sample collection systems for drugs of abuse testing.
Title 21 published on 2015-04-01.
No entries appear in the Federal Register after this date, for 21 CFR Part 809.