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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Part 809 — IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Subpart B — Labeling
Federal (United States) · Regulations
Subpart B — Labeling
2 sections
2 sections
21 C.F.R. § 809.10
Labeling for in vitro diagnostic products.
21 C.F.R. § 809.11
Exceptions or alternatives to labeling requirements for in vitro diagnostic products for human use held by the Strategic National Stockpile.
Subpart B — Labeling | Federal (United States) Regulations | Justis AI