US PART A — DRUGS AND DEVICES
- § 351. — Adulterated drugs and devices.
- § 352. — Misbranded drugs and devices.
- § 353. — Exemptions and consideration for certain drugs, devices, and biological products.
- § 353a. — Pharmacy compounding.
- § 354. — Veterinary feed directive drugs.
- § 355. — New drugs.
- § 355a. — Pediatric studies of drugs.
- § 356. — Fast track products.
- § 356a. — Manufacturing changes.
- § 356b. — Reports of postmarketing studies.
- § 356c. — Discontinuance of life saving product.
- § 357. — Repealed.
- § 358. — Authority to designate official names.
- § 359. — Nonapplicability of subchapter to cosmetics.
- § 360. — Registration of producers of drugs or devices.
- § 360a. — Repealed.
- § 360b. — New animal drugs.
- § 360c. — Classification of devices intended for human use.
- § 360d. — Performance standards.
- § 360e. — Premarket approval.
- § 360f. — Banned devices.
- § 360g. — Judicial review.
- § 360h. — Notification and other remedies.
- § 360i. — Records and reports on devices.
- § 360j. — General provisions respecting control of devices intended for human use.
- § 360k. — State and local requirements respecting devices.
- § 360l. — Postmarket surveillance.
- § 360m. — Accredited persons.