Title 21

Volume 8 CHAPTER I

Chapter I - Food And Drug Administration, Department Of Health And Human Services (continued)

CHAPTER I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

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