Topic

Medical devices

Every regulation in the Vantage corpus tagged with medical-devices. Items are tagged by the enrichment cron once they land, plus any topic attribution the connector pre-populates.

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US21 CFR21 CFR Part 99Secondary legislationIn force

Dissemination of Information on Unapproved/New Uses for Marketed Drugs, Biologics, and Devices

US21 CFR21 CFR Part 369Secondary legislationIn force

Interpretative Statements Re Warnings on Drugs and Devices for Over-the-Counter Sale

US21 CFR21 CFR Part 315Secondary legislationIn force

Diagnostic Radiopharmaceuticals

US21 CFR21 CFR Part 806Secondary legislationIn force

Medical Devices; Reports of Corrections and Removals

US21 CFR21 CFR Part 812Secondary legislationIn force

Investigational Device Exemptions

US21 CFR21 CFR Part 808Secondary legislationIn force

Exemptions from Federal Preemption of State and Local Medical Device Requirements

US21 CFR21 CFR Part 810Secondary legislationIn force

Medical Device Recall Authority

US21 CFR21 CFR Part 821Secondary legislationIn force

Medical Device Tracking Requirements

US21 CFR21 CFR Part 860Secondary legislationIn force

Medical Device Classification Procedures

US21 CFR21 CFR Part 814Secondary legislationIn force

Premarket Approval of Medical Devices

US21 CFR21 CFR Part 864Secondary legislationIn force

Hematology and Pathology Devices

US21 CFR21 CFR Part 866Secondary legislationIn force

Immunology and Microbiology Devices

US21 CFR21 CFR Part 874Secondary legislationIn force

Ear, Nose, and Throat Devices

US21 CFR21 CFR Part 868Secondary legislationIn force

Anesthesiology Devices

US21 CFR21 CFR Part 862Secondary legislationIn force

Clinical Chemistry and Clinical Toxicology Devices

US21 CFR21 CFR Part 872Secondary legislationIn force

Dental Devices

US21 CFR21 CFR Part 870Secondary legislationIn force

Cardiovascular Devices

US21 CFR21 CFR Part 876Secondary legislationIn force

Gastroenterology-Urology Devices

US21 CFR21 CFR Part 878Secondary legislationIn force

General and Plastic Surgery Devices

US21 CFR21 CFR Part 886Secondary legislationIn force

Ophthalmic Devices

US21 CFR21 CFR Part 884Secondary legislationIn force

Obstetrical and Gynecological Devices

US21 CFR21 CFR Part 882Secondary legislationIn force

Neurological Devices

US21 CFR21 CFR Part 895Secondary legislationIn force

Banned Devices

US21 CFR21 CFR Part 900Secondary legislationIn force

Mammography

US21 CFR21 CFR Part 890Secondary legislationIn force

Physical Medicine Devices

US21 CFR21 CFR Part 892Secondary legislationIn force

Radiology Devices

US21 CFR21 CFR Part 830Secondary legislationIn force

Unique Device Identification

US21 CFR21 CFR Part 809Secondary legislationIn force

In Vitro Diagnostic Products for Human Use

US21 CFR21 CFR Part 888Secondary legislationIn force

Orthopedic Devices

US21 CFR21 CFR Part 880Secondary legislationIn force

General Hospital and Personal Use Devices

US21 CFR21 CFR Part 660Secondary legislationIn force

Additional Standards for Diagnostic Substances for Laboratory Tests

US21 CFR21 CFR Part 607Secondary legislationIn force

Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices

US21 CFR21 CFR Part 803Secondary legislationIn force

Medical Device Reporting

US21 CFR21 CFR Part 807Secondary legislationIn force

Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices