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| 21:8.0.1.1 | SUBCHAP H
| SUBCHAPTER H - MEDICAL DEVICES | |
| 21:8.0.1.1.1 | PART 800
| PART 800 - GENERAL | |
| 21:8.0.1.1.2 | PART 801
| PART 801 - LABELING | |
| 21:8.0.1.1.3 | PART 803
| PART 803 - MEDICAL DEVICE REPORTING | |
| 21:8.0.1.1.4 | PART 806
| PART 806 - MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS | |
| 21:8.0.1.1.5 | PART 807
| PART 807 - ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES | |
| 21:8.0.1.1.6 | PART 808
| PART 808 - EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS | |
| 21:8.0.1.1.7 | PART 809
| PART 809 - IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE | |
| 21:8.0.1.1.8 | PART 810
| PART 810 - MEDICAL DEVICE RECALL AUTHORITY | |
| 21:8.0.1.1.9 | PART 812
| PART 812 - INVESTIGATIONAL DEVICE EXEMPTIONS | |
| 21:8.0.1.1.10 | PART 813
| PART 813 [RESERVED] | |
| 21:8.0.1.1.11 | PART 814
| PART 814 - PREMARKET APPROVAL OF MEDICAL DEVICES | |
| 21:8.0.1.1.12 | PART 820
| PART 820 - QUALITY SYSTEM REGULATION | |
| 21:8.0.1.1.13 | PART 821
| PART 821 - MEDICAL DEVICE TRACKING REQUIREMENTS | |
| 21:8.0.1.1.14 | PART 822
| PART 822 - POSTMARKET SURVEILLANCE | |
| 21:8.0.1.1.15 | PART 830
| PART 830 - UNIQUE DEVICE IDENTIFICATION | |
| 21:8.0.1.1.16 | PART 860
| PART 860 - MEDICAL DEVICE CLASSIFICATION PROCEDURES | |
| 21:8.0.1.1.17 | PART 861
| PART 861 - PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT | |
| 21:8.0.1.1.18 | PART 862
| PART 862 - CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES | |
| 21:8.0.1.1.19 | PART 864
| PART 864 - HEMATOLOGY AND PATHOLOGY DEVICES | |
| 21:8.0.1.1.20 | PART 866
| PART 866 - IMMUNOLOGY AND MICROBIOLOGY DEVICES | |
| 21:8.0.1.1.21 | PART 868
| PART 868 - ANESTHESIOLOGY DEVICES | |
| 21:8.0.1.1.22 | PART 870
| PART 870 - CARDIOVASCULAR DEVICES | |
| 21:8.0.1.1.23 | PART 872
| PART 872 - DENTAL DEVICES | |
| 21:8.0.1.1.24 | PART 874
| PART 874 - EAR, NOSE, AND THROAT DEVICES | |
| 21:8.0.1.1.25 | PART 876
| PART 876 - GASTROENTEROLOGY-UROLOGY DEVICES | |
| 21:8.0.1.1.26 | PART 878
| PART 878 - GENERAL AND PLASTIC SURGERY DEVICES | |
| 21:8.0.1.1.27 | PART 880
| PART 880 - GENERAL HOSPITAL AND PERSONAL USE DEVICES | |
| 21:8.0.1.1.28 | PART 882
| PART 882 - NEUROLOGICAL DEVICES | |
| 21:8.0.1.1.29 | PART 884
| PART 884 - OBSTETRICAL AND GYNECOLOGICAL DEVICES | |
| 21:8.0.1.1.30 | PART 886
| PART 886 - OPHTHALMIC DEVICES | |
| 21:8.0.1.1.31 | PART 888
| PART 888 - ORTHOPEDIC DEVICES | |
| 21:8.0.1.1.32 | PART 890
| PART 890 - PHYSICAL MEDICINE DEVICES | |
| 21:8.0.1.1.33 | PART 892
| PART 892 - RADIOLOGY DEVICES | |
| 21:8.0.1.1.34 | PART 895
| PART 895 - BANNED DEVICES | |
| 21:8.0.1.1.35 | PART 898
| PART 898 - PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES | |
| 21:8.0.1.2 | SUBCHAP I
| SUBCHAPTER I - MAMMOGRAPHY QUALITY STANDARDS ACT | |
| 21:8.0.1.2.36 | PART 900
| PART 900 - MAMMOGRAPHY | |
| 21:8.0.1.3 | SUBCHAP J
| SUBCHAPTER J - RADIOLOGICAL HEALTH | |
| 21:8.0.1.3.37 | PART 1000
| PART 1000 - GENERAL | |
| 21:8.0.1.3.38 | PART 1002
| PART 1002 - RECORDS AND REPORTS | |
| 21:8.0.1.3.39 | PART 1003
| PART 1003 - NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY | |
| 21:8.0.1.3.40 | PART 1004
| PART 1004 - REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS | |
| 21:8.0.1.3.41 | PART 1005
| PART 1005 - IMPORTATION OF ELECTRONIC PRODUCTS | |
| 21:8.0.1.3.42 | PART 1010
| PART 1010 - PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL | |
| 21:8.0.1.3.43 | PART 1020
| PART 1020 - PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS | |
| 21:8.0.1.3.44 | PART 1030
| PART 1030 - PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS | |
| 21:8.0.1.3.45 | PART 1040
| PART 1040 - PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS | |
| 21:8.0.1.3.46 | PART 1050
| PART 1050 - PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS | |
| 21:8.0.1.4 | SUBCHAP K
| SUBCHAPTER K - TOBACCO PRODUCTS | |
| 21:8.0.1.4.47 | PART 1100
| PART 1100 - TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY | |
| 21:8.0.1.4.48 | PART 1105
| PART 1105 - GENERAL | |
| 21:8.0.1.4.49 | PART 1107
| PART 1107 - ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS | |
| 21:8.0.1.4.50 | PART 1140
| PART 1140 - CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS | |
| 21:8.0.1.4.51 | PART 1141
| PART 1141 - CIGARETTE PACKAGE AND ADVERTISING WARNINGS | |
| 21:8.0.1.4.52 | PART 1143
| PART 1143 - MINIMUM REQUIRED WARNING STATEMENTS | |
| 21:8.0.1.4.53 | PART 1150
| PART 1150 - USER FEES | |
| 21:8.0.1.5 | SUBCHAP L
| SUBCHAPTER L - REGULATIONS UNDER CERTAIN OTHER ACTS ADMINISTERED BY THE FOOD AND DRUG ADMINISTRATION | |
| 21:8.0.1.5.54 | PART 1210
| PART 1210 - REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT | |
| 21:8.0.1.5.55 | PART 1230
| PART 1230 - REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT | |
| 21:8.0.1.5.56 | PART 1240
| PART 1240 - CONTROL OF COMMUNICABLE DISEASES | |
| 21:8.0.1.5.57 | PART 1250
| PART 1250 - INTERSTATE CONVEYANCE SANITATION | |
| 21:8.0.1.5.58 | PART 1251-1269
| PARTS 1251-1269 [RESERVED] | |
| 21:8.0.1.5.59 | PART 1270
| PART 1270 - HUMAN TISSUE INTENDED FOR TRANSPLANTATION | |
| 21:8.0.1.5.60 | PART 1271
| PART 1271 - HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS | |
| 21:8.0.1.5.61 | PART 1272-1299
| PARTS 1272-1299 [RESERVED] | |