Monitoring Gesetzessammlung

Gesetze und Verordnungen USA alphabetisch

A B C D E F G H I J
K L M N O P Q R S T
U V W X Y Z
0 1 2 3 4 5 6 7 8 9
PART 80—COLOR ADDITIVE CERTIFICATION
21 CFR Part 80
PART 800—GENERAL
21 CFR Part 800
PART 801—LABELING
21 CFR Part 801
PART 803—MEDICAL DEVICE REPORTING
21 CFR Part 803
PART 806—MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
21 CFR Part 806
PART 807—ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
21 CFR Part 807
PART 808—EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
21 CFR Part 808
PART 809—IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
21 CFR Part 809
PART 81—GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS
21 CFR Part 81
PART 810—MEDICAL DEVICE RECALL AUTHORITY
21 CFR Part 810
PART 812—INVESTIGATIONAL DEVICE EXEMPTIONS
21 CFR Part 812
PART 814—PREMARKET APPROVAL OF MEDICAL DEVICES
21 CFR Part 814
PART 82—LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS
21 CFR Part 82
PART 820—QUALITY MANAGEMENT SYSTEM REGULATION
21 CFR Part 820
PART 821—MEDICAL DEVICE TRACKING REQUIREMENTS
21 CFR Part 821
PART 822—POSTMARKET SURVEILLANCE
21 CFR Part 822
PART 830—UNIQUE DEVICE IDENTIFICATION
21 CFR Part 830
PART 860—MEDICAL DEVICE CLASSIFICATION PROCEDURES
21 CFR Part 860
PART 861—PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
21 CFR Part 861
PART 862—CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
21 CFR Part 862
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