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20 results 360e-1
Scoped to Title 21
Exact match Title 21 Title 21 / Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices / Section 360e–1

21 U.S.C. § 360e–1

Pediatric uses of devices

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Exact citation match for 21 USC § 360E-1

Title 21 Title 21 / Section 301

21 U.S.C. § 301

Short title

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter I SHORT TITLE

Short title

Title 21 Title 21 / Section 379j–1

21 U.S.C. § 379j–1

Reauthorization; reporting requirements

Part C Fees / Subpart 3 fees relating to devices

Reauthorization; reporting requirements

Title 21 Title 21 / Section 360g

21 U.S.C. § 360g

Judicial review

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Judicial review

Title 21 Title 21 / Section 360c

21 U.S.C. § 360c

Classification of devices intended for human use

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Classification of devices intended for human use

Title 21 Title 21 / Section 360j

21 U.S.C. § 360j

General provisions respecting control of devices intended for human use

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

General provisions respecting control of devices intended for human use

Title 21 Title 21 / Section 356–1

21 U.S.C. § 356–1

Accelerated approval of priority countermeasures

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Accelerated approval of priority countermeasures

Title 21 Title 21 / Section 360m

21 U.S.C. § 360m

Accredited persons

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Accredited persons

Title 21 Title 21 / Section 360e–4

21 U.S.C. § 360e–4

Predetermined change control plans for devices

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Predetermined change control plans for devices

Title 21 Title 21 / Section 360e

21 U.S.C. § 360e

Premarket approval

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Premarket approval

Title 21 Title 21 / Section 360c–1

21 U.S.C. § 360c–1

Reporting

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Reporting

Title 21 Title 21 / Section 360e–3

21 U.S.C. § 360e–3

Breakthrough devices

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Breakthrough devices

Title 21 Title 21 / Section 360g–1

21 U.S.C. § 360g–1

Agency documentation and review of significant decisions regarding devices

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Agency documentation and review of significant decisions regarding devices

Title 21 Title 21 / Section 360bbb–1

21 U.S.C. § 360bbb–1

Dispute resolution

Subchapter V DRUGS AND DEVICES / Part E General Provisions Relating to Drugs and Devices

Dispute resolution

Title 21 Title 21 / Section 379k–1

21 U.S.C. § 379k–1

Electronic format for submissions

Subchapter VII GENERAL AUTHORITY / Part D Information and Education

Electronic format for submissions

Title 21 Title 21 / Section 379i

21 U.S.C. § 379i

Definitions

Part C Fees / Subpart 3 fees relating to devices

Definitions

Title 21 Title 21 / Section 360l

21 U.S.C. § 360l

Postmarket surveillance

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Postmarket surveillance

Title 21 Title 21 / Section 360rr

21 U.S.C. § 360rr

Federal-State cooperation

Subchapter V DRUGS AND DEVICES / Part C Electronic Product Radiation Control

Federal-State cooperation

Title 21 Title 21 / Section 360bbb–3

21 U.S.C. § 360bbb–3

Authorization for medical products for use in emergencies

Subchapter V DRUGS AND DEVICES / Part E General Provisions Relating to Drugs and Devices

Authorization for medical products for use in emergencies

Title 21 Title 21 / Section 360bbb–3c

21 U.S.C. § 360bbb–3c

Expedited development and review of medical products for emergency uses

Subchapter V DRUGS AND DEVICES / Part E General Provisions Relating to Drugs and Devices

Expedited development and review of medical products for emergency uses