CFR 21(PTS500-599) : 0
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 500-599
20-11-2019
Part 500 - General
Part 501 - Animal food labeling
Part 502 - Common or usual names for nonstandardized animal
foods
Part 509 - Unavoidable contaminants in animal food and food-
packaging material
Part 510 - New animal drugs
Part 511 - New animal drugs for investigational use
Part 514 - New animal drug applications
Part 515 - Medicated feed mill license
Part 520 - Oral dosage form new animal drugs
Part 522 - Implantation or injectable dosage form new animal drugs
Part 524 - Ophthalmic and topical dosage form new animal drugs
Part 526 - Intramammary dosage forms
Part 529 - Certain other dosage form new animal drugs
Part 530 - Extralabel drug use in animals
Part 556 - Tolerances for residues of new animal drugs in food
Part 558 - New animal drugs for use in animal feeds
Part 564 - [Reserved]
Part 570 - Food additives
Part 571 - Food additive petitions
Part 573 - Food additives permitted in feed and drinking water of
animals
Part 579 - Irradiation in the production, processing, and handling
of animal feed and pet food
Part 582 - Substances generally recognized as safe
Part 584 - Food substances affirmed as generally recognized as safe in
feed and drinking water of animals
Part 589 - Substances prohibited from use in animal food or feed
Part 590-599 - [Reserved]
| DocumentType |
Standard
|
| PublisherName |
Code of Federal Regulations
|
| Status |
Superseded
|
| SupersededBy |
| ANSI/AAMI/IEC 60601-1-2:2014 | MEDICAL ELECTRICAL EQUIPMENT - PART 1-2: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: ELECTROMAGNETIC DISTURBANCES - REQUIREMENTS AND TESTS |
| DD ISO/TS 22224:2009 | Health informatics. Electronic reporting of adverse drug reactions |
| DI-TCSP-82040 Base Document:2016 | RESEARCH AND DEVELOPMENT OF MEDICAL PRODUCTS REGULATED BY THE U.S. FOOD AND DRUG ADMINISTRATION (FDA) |
| ISO/TS 22224:2009 | Health informatics Electronic reporting of adverse drug reactions |
| IEC 60601-1-2:2007 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests |
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