Chapter I-i 7. SUBCHAPTER H—MEDICAL DEVICES

• 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 - § 820.45] - PART 820—QUALITY MANAGEMENT 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 - § 892.6510] - 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]