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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 607 — ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
Subpart E — Establishment Registration and Product Listing Of Licensed Devices
Federal (United States) · Regulations
Subpart E — Establishment Registration and Product Listing Of Licensed Devices
1 section
1 section
21 C.F.R. § 607.80
Applicability of part 607 to licensed devices.
Subpart E — Establishment Registration and Product Listing Of Licensed Devices | Federal (United States) Regulations | Justis AI