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  • Sec.  351. Adulterated drugs and devices.
  • Sec.  352. Misbranded drugs and devices.
  • Sec.  353. Exemptions and consideration for certain drugs, devices, and biological products.
  • Sec.  353a. Pharmacy compounding.
  • Sec.  354. Veterinary feed directive drugs.
  • Sec.  355. New drugs.
  • Sec.  355a. Pediatric studies of drugs.
  • Sec.  356. Fast track products.
  • Sec.  356a. Manufacturing changes.
  • Sec.  356b. Reports of postmarketing studies.
  • Sec.  356c. Discontinuance of life saving product.
  • Sec.  357. Repealed.
  • Sec.  358. Authority to designate official names.
  • Sec.  359. Nonapplicability of subchapter to cosmetics.
  • Sec.  360. Registration of producers of drugs or devices.
  • Sec.  360a. Repealed.
  • Sec.  360b. New animal drugs.
  • Sec.  360c. Classification of devices intended for human use.
  • Sec.  360d. Performance standards.
  • Sec.  360e. Premarket approval.
  • Sec.  360f. Banned devices.
  • Sec.  360g. Judicial review.
  • Sec.  360h. Notification and other remedies.
  • Sec.  360i. Records and reports on devices.
  • Sec.  360j. General provisions respecting control of devices intended for human use.
  • Sec.  360k. State and local requirements respecting devices.
  • Sec.  360l. Postmarket surveillance.
  • Sec.  360m. Accredited persons.
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(Last updated May 8, 2002)