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Title 21
Title 21 / Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices / Section 360c–1
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360c-1
Scoped to Title 21
Title 21
Title 21 / Section 360c
21 U.S.C. § 360c
Classification of devices intended for human use
Classification of devices intended for human use
Title 21
Title 21 / Section 360g–1
21 U.S.C. § 360g–1
Agency documentation and review of significant decisions regarding devices
Agency documentation and review of significant decisions regarding devices
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Title 21 / Section 360m
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Title 21 / Section 360d
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Title 21 / Section 360
21 U.S.C. § 360
Registration of producers of drugs or devices
Registration of producers of drugs or devices
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Title 21 / Section 360j
21 U.S.C. § 360j
General provisions respecting control of devices intended for human use
General provisions respecting control of devices intended for human use
Title 21
Title 21 / Section 353
21 U.S.C. § 353
Exemptions and consideration for certain drugs, devices, and biological products
Exemptions and consideration for certain drugs, devices, and biological products
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Title 21 / Section 379k–1
Title 21
Title 21 / Section 360e
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Title 21 / Section 360g
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Title 21 / Section 379i
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Title 21 / Section 360e–4
21 U.S.C. § 360e–4
Predetermined change control plans for devices
Predetermined change control plans for devices
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Title 21 / Section 352
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Title 21 / Section 360a–2
21 U.S.C. § 360a–2
Susceptibility test interpretive criteria for microorganisms
Susceptibility test interpretive criteria for microorganisms
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Title 21 / Section 360n–2
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Title 21 / Section 356j
21 U.S.C. § 356j
Discontinuance or interruption in the production of medical devices
Discontinuance or interruption in the production of medical devices
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Title 21 / Section 360bbb–3
21 U.S.C. § 360bbb–3
Authorization for medical products for use in emergencies
Authorization for medical products for use in emergencies
Title 21
Title 21 / Section 360bbb–4b
Title 21
Title 21 / Section 1604