Investigational Device Exemptions

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

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Subpart
A

General Provisions

Subpart
B

Application and Administrative Action

Subpart
C

Responsibilities of Sponsors

Subpart
D

IRB Review and Approval

Subpart
E

Responsibilities of Investigators

Subpart
F

Subpart F [Reserved]

Subpart
G

Records and Reports