21 CFR Subchapter H MEDICAL DEVICES | Code of Federal Regulations | US Law | LawStack Online

21 CFR Subchapter H

MEDICAL DEVICES

June 25, 2020

PREMARKET APPROVAL OF MEDICAL DEVICES

MEDICAL DEVICE REPORTING

ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES

MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS

EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS

IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE

MEDICAL DEVICE RECALL AUTHORITY

INVESTIGATIONAL DEVICE EXEMPTIONS

QUALITY SYSTEM REGULATION

MEDICAL DEVICE TRACKING REQUIREMENTS

POSTMARKET SURVEILLANCE

UNIQUE DEVICE IDENTIFICATION

MEDICAL DEVICE CLASSIFICATION PROCEDURES

PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT

CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES

HEMATOLOGY AND PATHOLOGY DEVICES

IMMUNOLOGY AND MICROBIOLOGY DEVICES

ANESTHESIOLOGY DEVICES

CARDIOVASCULAR DEVICES

EAR, NOSE, AND THROAT DEVICES

GASTROENTEROLOGY-UROLOGY DEVICES

GENERAL AND PLASTIC SURGERY DEVICES

GENERAL HOSPITAL AND PERSONAL USE DEVICES

NEUROLOGICAL DEVICES

OBSTETRICAL AND GYNECOLOGICAL DEVICES

OPHTHALMIC DEVICES

ORTHOPEDIC DEVICES

PHYSICAL MEDICINE DEVICES

RADIOLOGY DEVICES

PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES

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