FDA
MEDICAL DEVICES
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Table of
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Headings |
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| MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS |
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| ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES |
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| EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS |
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| IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE |
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| MEDICAL DEVICE RECALL AUTHORITY |
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| INVESTIGATIONAL DEVICE EXEMPTIONS |
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| PREMARKET APPROVAL OF MEDICAL DEVICES |
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| QUALITY SYSTEM REGULATION |
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| MEDICAL DEVICE TRACKING REQUIREMENTS |
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| UNIQUE DEVICE IDENTIFICATION |
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| MEDICAL DEVICE CLASSIFICATION PROCEDURES |
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| PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT |
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| CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES |
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| HEMATOLOGY AND PATHOLOGY DEVICES |
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| IMMUNOLOGY AND MICROBIOLOGY DEVICES |
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| EAR, NOSE, AND THROAT DEVICES |
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| GASTROENTEROLOGY-UROLOGY DEVICES |
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| GENERAL AND PLASTIC SURGERY DEVICES |
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| GENERAL HOSPITAL AND PERSONAL USE DEVICES |
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| OBSTETRICAL AND GYNECOLOGICAL DEVICES |
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| PHYSICAL MEDICINE DEVICES |
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| PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES |
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SUBCHAPTER I—MAMMOGRAPHY QUALITY STANDARDS ACT
SUBCHAPTER J—RADIOLOGICAL HEALTH
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| NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY |
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| REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS |
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| IMPORTATION OF ELECTRONIC PRODUCTS |
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| PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL |
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| PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS |
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| PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS |
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| PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS |
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| PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS |
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SUBCHAPTER K—TOBACCO PRODUCTS
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| TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY |
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| ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS |
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| CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS |
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| CIGARETTE PACKAGE AND ADVERTISING WARNINGS |
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| MINIMUM REQUIRED WARNING STATEMENTS |
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SUBCHAPTER L—REGULATIONS UNDER CERTAIN OTHER ACTS ADMINISTERED BY THE FOOD AND DRUG ADMINISTRATION
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| REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT |
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| REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT |
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| CONTROL OF COMMUNICABLE DISEASES |
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| INTERSTATE CONVEYANCE SANITATION |
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| HUMAN TISSUE INTENDED FOR TRANSPLANTATION |
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| HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS |
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