• 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 - § 862.3950] - PART 862—CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES

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

• Part 866 [§ 866.1 - § 866.6080] - 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]