Code of Federal Regulations > Title 21 > Chapter I - CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

U.S. Code of Federal Regulations

Regulations most recently checked for updates: May 13, 2025

Part 800 [§ 800.10 - § 800.75] - PART 800—GENERAL

Part 801 [§ 801.1 - § 801.437] - PART 801—LABELING

Part 803 [§ 803.1 - § 803.58] - PART 803—MEDICAL DEVICE REPORTING

Part 806 [§ 806.1 - § 806.40] - PART 806—MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS

Part 807 [§ 807.3 - § 807.100] - PART 807—ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES

Part 808 [§ 808.1 - § 808.57—808.101] - PART 808—EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS

Part 809 [§ 809.3 - § 809.40] - PART 809—IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE

Part 810 [§ 810.1 - § 810.18] - PART 810—MEDICAL DEVICE RECALL AUTHORITY

Part 812 [§ 812.1 - § 812.150] - PART 812—INVESTIGATIONAL DEVICE EXEMPTIONS

Part 813 - PART 813 [RESERVED]

Part 814 [§ 814.1 - § 814.126] - PART 814—PREMARKET APPROVAL OF MEDICAL DEVICES

Part 820 [§ 820.1 - § 820.250] - PART 820—QUALITY SYSTEM REGULATION

Part 821 [§ 821.1 - § 821.60] - PART 821—MEDICAL DEVICE TRACKING REQUIREMENTS

Part 822 [§ 822.1 - § 822.38] - PART 822—POSTMARKET SURVEILLANCE

Part 830 [§ 830.3 - § 830.360] - PART 830—UNIQUE DEVICE IDENTIFICATION

Part 860 [§ 860.1 - § 860.260] - PART 860—MEDICAL DEVICE CLASSIFICATION PROCEDURES

Part 861 [§ 861.1 - § 861.38] - PART 861—PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT

Part 862 [§ 862.1 - § 862.3970] - PART 862—CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES

Part 864 [§ 864.1 - § 864.9900] - PART 864—HEMATOLOGY AND PATHOLOGY DEVICES

Part 866 [§ 866.1 - § 866.6100] - PART 866—IMMUNOLOGY AND MICROBIOLOGY DEVICES

Part 868 [§ 868.1 - § 868.6885] - PART 868—ANESTHESIOLOGY DEVICES

Part 870 [§ 870.1 - § 870.5925] - PART 870—CARDIOVASCULAR DEVICES

Part 872 [§ 872.1 - § 872.6890] - PART 872—DENTAL DEVICES

Part 874 [§ 874.1 - § 874.5900] - PART 874—EAR, NOSE, AND THROAT DEVICES

Part 876 [§ 876.1 - § 876.5990] - PART 876—GASTROENTEROLOGY-UROLOGY DEVICES

Part 878 [§ 878.1 - § 878.5910] - PART 878—GENERAL AND PLASTIC SURGERY DEVICES

Part 880 [§ 880.1 - § 880.6992] - PART 880—GENERAL HOSPITAL AND PERSONAL USE DEVICES

Part 882 [§ 882.1 - § 882.5970] - PART 882—NEUROLOGICAL DEVICES

Part 884 [§ 884.1 - § 884.6200] - PART 884—OBSTETRICAL AND GYNECOLOGICAL DEVICES

Part 886 [§ 886.1 - § 886.5933] - PART 886—OPHTHALMIC DEVICES

Part 888 [§ 888.1 - § 888.5980] - PART 888—ORTHOPEDIC DEVICES

Part 890 [§ 890.1 - § 890.5975] - PART 890—PHYSICAL MEDICINE DEVICES

Part 892 [§ 892.1 - § 892.6500] - PART 892—RADIOLOGY DEVICES

Part 895 [§ 895.1 - § 895.105] - PART 895—BANNED DEVICES

Part 898 [§ 898.11 - § 898.14] - PART 898—PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES

Part 900 [§ 900.1 - § 900.25] - PART 900—MAMMOGRAPHY

Part 1000 [§ 1000.1 - § 1000.15] - PART 1000—GENERAL

Part 1002 [§ 1002.1 - § 1002.51] - PART 1002—RECORDS AND REPORTS

Part 1003 [§ 1003.1 - § 1003.31] - PART 1003—NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY

Part 1004 [§ 1004.1 - § 1004.6] - PART 1004—REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS

Part 1005 [§ 1005.1 - § 1005.25] - PART 1005—IMPORTATION OF ELECTRONIC PRODUCTS

Part 1010 [§ 1010.1 - § 1010.20] - PART 1010—PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL

Part 1020 [§ 1020.10 - § 1020.40] - PART 1020—PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS

Part 1030 [§ 1030.10 - § 1030.10] - PART 1030—PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS

Part 1040 [§ 1040.10 - § 1040.30] - PART 1040—PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS

Part 1100 [§ 1100.1 - § 1100.204] - PART 1100—General

Part 1105 [§ 1105.10 - § 1105.10] - PART 1105—GENERAL

Part 1107 [§ 1107.1 - § 1107.62] - PART 1107—EXEMPTION REQUESTS AND SUBSTANTIAL EQUIVALENCE REPORTS

Part 1114 [§ 1114.1 - § 1114.49] - PART 1114—PREMARKET TOBACCO PRODUCT APPLICATIONS

Part 1140 [§ 1140.1 - § 1140.34] - PART 1140—CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS

Part 1141 [§ 1141.1 - § 1141.12] - PART 1141—REQUIRED WARNINGS FOR CIGARETTE PACKAGES AND ADVERTISEMENTS

Part 1143 [§ 1143.1 - § 1143.13] - PART 1143—MINIMUM REQUIRED WARNING STATEMENTS

Part 1150 [§ 1150.1 - § 1150.17] - PART 1150—USER FEES

Part 1210 [§ 1210.1 - § 1210.31] - PART 1210—REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT

Part 1230 [§ 1230.2 - § 1230.49] - PART 1230—REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT

Part 1240 [§ 1240.3 - § 1240.95] - PART 1240—CONTROL OF COMMUNICABLE DISEASES

Part 1250 [§ 1250.3 - § 1250.96] - PART 1250—INTERSTATE CONVEYANCE SANITATION

Part 1251-1270 - PARTS 1251-1270 [RESERVED]

Part 1271 [§ 1271.1 - § 1271.440] - PART 1271—HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS

Part 1272-1299 - PARTS 1272-1299 [RESERVED]