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Title 21 - Food and Drugs
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CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
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SUBCHAPTER H—MEDICAL DEVICES (parts 800 to 898)
CFR
Title 1 - General Provisions
Title 2 - Grants and Agreements
Title 3 - The President
Title 4 - Accounts
Title 5 - Administrative Personnel
Title 6 - Domestic Security
Title 7 - Agriculture
Title 8 - Aliens and Nationality
Title 9 - Animals and Animal Products
Title 10 - Energy
Title 11 - Federal Elections
Title 12 - Banks and Banking
Title 13 - Business Credit and Assistance
Title 14 - Aeronautics and Space
Title 15 - Commerce and Foreign Trade
Title 16 - Commercial Practices
Title 17 - Commodity and Securities Exchanges
Title 18 - Conservation of Power and Water Resources
Title 19 - Customs Duties
Title 20 - Employees' Benefits
Title 21 - Food and Drugs
Title 22 - Foreign Relations
Title 23 - Highways
Title 24 - Housing and Urban Development
Title 25 - Indians
Title 26 - Internal Revenue
Title 27 - Alcohol, Tobacco Products and Firearms
Title 28 - Judicial Administration
Title 29 - Labor
Title 30 - Mineral Resources
Title 31 - Money and Finance: Treasury
Title 32 - National Defense
Title 33 - Navigation and Navigable Waters
Title 34 - Education
Title 35 - Panama Canal
Title 36 - Parks, Forests, and Public Property
Title 37 - Patents, Trademarks, and Copyrights
Title 38 - Pensions, Bonuses, and Veterans' Relief
Title 39 - Postal Service
Title 40 - Protection of Environment
Title 41 - Public Contracts and Property Management
Title 42 - Public Health
Title 43 - Public Lands: Interior
Title 44 - Emergency Management and Assistance
Title 45 - Public Welfare
Title 46 - Shipping
Title 47 - Telecommunication
Title 48 - Federal Acquisition Regulations System
Title 49 - Transportation
Title 50 - Wildlife and Fisheries
SUBCHAPTER H—MEDICAL DEVICES (parts 800 to 898)
PART 800—GENERAL
PART 801—LABELING
PART 803—MEDICAL DEVICE REPORTING
PART 806—MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
PART 807—ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
PART 808—EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
PART 809—IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
PART 810—MEDICAL DEVICE RECALL AUTHORITY
PART 812—INVESTIGATIONAL DEVICE EXEMPTIONS
PART 814—PREMARKET APPROVAL OF MEDICAL DEVICES
PART 820—QUALITY SYSTEM REGULATION
PART 821—MEDICAL DEVICE TRACKING REQUIREMENTS
PART 822—POSTMARKET SURVEILLANCE
PART 860—MEDICAL DEVICE CLASSIFICATION PROCEDURES
PART 861—PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
PART 862—CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
PART 864—HEMATOLOGY AND PATHOLOGY DEVICES
PART 866—IMMUNOLOGY AND MICROBIOLOGY DEVICES
PART 868—ANESTHESIOLOGY DEVICES
PART 870—CARDIOVASCULAR DEVICES
PART 872—DENTAL DEVICES
PART 874—EAR, NOSE, AND THROAT DEVICES
PART 876—GASTROENTEROLOGY-UROLOGY DEVICES
PART 878—GENERAL AND PLASTIC SURGERY DEVICES
PART 880—GENERAL HOSPITAL AND PERSONAL USE DEVICES
PART 882—NEUROLOGICAL DEVICES
PART 884—OBSTETRICAL AND GYNECOLOGICAL DEVICES
PART 886—OPHTHALMIC DEVICES
PART 888—ORTHOPEDIC DEVICES
PART 890—PHYSICAL MEDICINE DEVICES
PART 892—RADIOLOGY DEVICES
PART 895—BANNED DEVICES
PART 898—PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
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