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21 U.S.C. 352 - Misbranded drugs and devices

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Publication TitleMouse over help for Publication Title says The title of the publication. Sections within the United States Code can be searched using the title field operator. Search field operator example is title:"coral reef conservation program".United States Code, 2006 Edition, Supplement 4, Title 21 - FOOD AND DRUGS
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CollectionMouse over help for Collection says The collection to which the document belongs. Typically the same as the publication or series. Search field operator example is collection:uscode.United States Code
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Contained WithinMouse over help for Contained Within says The document hierarchicy for a U.S. Code document. Search field operator example is title:"Flag and Seal Seat of Government and the States".Title 21 - FOOD AND DRUGS
CHAPTER 9 - FEDERAL FOOD, DRUG, AND COSMETIC ACT
SUBCHAPTER V - DRUGS AND DEVICES
Part A - Drugs and Devices
Sec. 352 - Misbranded drugs and devices
ContainsMouse over help for Contains says The U.S. Code sections contained within the document. section 352
DateMouse over help for Date says The edition of the U.S. Code. 2010
Laws in Effect as of DateMouse over help for Laws in Effect as of Date says The date by which laws were included in this edition of the U.S. Code. This edition of the U.S. Code does not include laws that went into effect after this date.January 7, 2011
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53 Stat. 854, 853
55 Stat. 851
59 Stat. 463
61 Stat. 11
63 Stat. 409
67 Stat. 389
74 Stat. 398
76 Stat. 785
79 Stat. 234
82 Stat. 352
84 Stat. 1673
90 Stat. 577
92 Stat. 3773
95 Stat. 716
106 Stat. 239, 4499
107 Stat. 777
111 Stat. 2325, 2327, 2312
116 Stat. 1613, 1616
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124 Stat. 530
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Document in Context
   
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Table Of Contents
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Table Of Contents
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Front Matter
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Sec. 351 - Adulterated drugs and devices
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Sec. 352 - Misbranded drugs and devices
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Sec. 353 - Exemptions and consideration for certain drugs, devices, and biological products
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Sec. 353a - Pharmacy compounding
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Sec. 353b - Prereview of television advertisements
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Sec. 354 - Veterinary feed directive drugs
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Sec. 355 - New drugs
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Sec. 355-1 - Risk evaluation and mitigation strategies
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Sec. 355a - Pediatric studies of drugs
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Sec. 355b - Adverse-event reporting
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Sec. 355c - Research into pediatric uses for drugs and biological products
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Sec. 355d - Internal committee for review of pediatric plans, assessments, deferrals, and waivers
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Sec. 355e - Pharmaceutical security
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Sec. 356 - Fast track products
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Sec. 356-1 - Accelerated approval of priority countermeasures
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Sec. 356a - Manufacturing changes
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Sec. 356b - Reports of postmarketing studies
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Sec. 356c - Discontinuance of life saving product
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Sec. 357 - Repealed. Pub. L. 105-115, title I, §125(b)(1), Nov. 21, 1997, 111 Stat. 2325
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Sec. 358 - Authority to designate official names
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Sec. 359 - Nonapplicability of subchapter to cosmetics
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Sec. 360 - Registration of producers of drugs or devices
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Sec. 360a - Clinical trial guidance for antibiotic drugs
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Sec. 360b - New animal drugs
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Sec. 360c - Classification of devices intended for human use
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Sec. 360d - Performance standards
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Sec. 360e - Premarket approval
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Sec. 360e-1 - Pediatric uses of devices
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Sec. 360f - Banned devices
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Sec. 360g - Judicial review
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Sec. 360h - Notification and other remedies
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Sec. 360i - Records and reports on devices
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Sec. 360j - General provisions respecting control of devices intended for human use
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Sec. 360k - State and local requirements respecting devices
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Sec. 360l - Postmarket surveillance
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Sec. 360m - Accredited persons
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Sec. 360n - Priority review to encourage treatments for tropical diseases
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