Medical Device User Fee and Modernization Act of 2002

Pub. L. 107-250

15 sections of the Code credited to this law, found between Public Law 107-136 and Public Law 107-377.

• 21 U.S.C. § 321 — Definitions; generally
• 21 U.S.C. § 331 — Prohibited acts
• 21 U.S.C. § 333 — Penalties
• 21 U.S.C. § 335a — Debarment, temporary denial of approval, and suspension
• 21 U.S.C. § 352 — Misbranded drugs and devices
• 21 U.S.C. § 353 — Exemptions and consideration for certain drugs, devices, and biological products
• 21 U.S.C. § 360 — Registration of producers of drugs or devices
• 21 U.S.C. § 360c — Classification of devices intended for human use
• 21 U.S.C. § 360e — Premarket approval
• 21 U.S.C. § 360m — Accredited persons
• 21 U.S.C. § 374 — Inspection
• 21 U.S.C. § 379i — Definitions
• 21 U.S.C. § 379j — Authority to assess and use device fees
• 42 U.S.C. § 289g-3 — 289g–3. Breast implant research
• 42 U.S.C. § 289g–3 — Breast implant research