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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
Federal (United States) · Regulations
Part 809 — IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
7 sections
3 groups
Subpart A — General Provisions
2 sections
Subpart B — Labeling
2 sections
Subpart C — Requirements for Manufacturers and Producers
3 sections
Part 809 — IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE | Federal (United States) Regulations | Justis AI