Labeling

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Medical Devices
  6. Labeling

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Subpart
A

General Labeling Provisions

Subpart
B

Labeling Requirements for Unique Device Identification

Subpart
C

Labeling Requirements for Over-the-Counter Devices

Subpart
D

Exemptions From Adequate Directions for Use

Subpart
E

Other Exemptions

Subpart
F-G

Subparts F-G [Reserved]

Subpart
H

Special Requirements for Specific Devices