---
kind: "unit"
title: "21"
title_heading: "Food and Drugs"
key: "chI/subchH"
level: "subchap"
label: "Subchapter H"
heading: "Medical Devices"
release: "ecfr-current"
date: "2026-08-27"
url: "https://uscodex.org/cfr/21/chI-subchH"
sections_count: 2533
---

# Subchapter H — Medical Devices

Title 21 C.F.R. — Food and Drugs › Chapter I — Food and Drug Administration, Department of Health and Human Services

## Contents

- [Part 800 — General](/cfr/21/chI-subchH-part800.md)
- [Part 801 — Labeling](/cfr/21/chI-subchH-part801.md)
- [Part 803 — Medical Device Reporting](/cfr/21/chI-subchH-part803.md)
- [Part 806 — Medical Devices; Reports of Corrections and Removals](/cfr/21/chI-subchH-part806.md)
- [Part 807 — Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices](/cfr/21/chI-subchH-part807.md)
- [Part 808 — Exemptions from Federal Preemption of State and Local Medical Device Requirements](/cfr/21/chI-subchH-part808.md)
- [Part 809 — In Vitro Diagnostic Products for Human Use](/cfr/21/chI-subchH-part809.md)
- [Part 810 — Medical Device Recall Authority](/cfr/21/chI-subchH-part810.md)
- [Part 812 — Investigational Device Exemptions](/cfr/21/chI-subchH-part812.md)
- [Part 813 — Part 813 [reserved]](/cfr/21/chI-subchH-part813.md)
- [Part 814 — Premarket Approval of Medical Devices](/cfr/21/chI-subchH-part814.md)
- [Part 820 — Quality Management System Regulation](/cfr/21/chI-subchH-part820.md)
- [Part 821 — Medical Device Tracking Requirements](/cfr/21/chI-subchH-part821.md)
- [Part 822 — Postmarket Surveillance](/cfr/21/chI-subchH-part822.md)
- [Part 830 — Unique Device Identification](/cfr/21/chI-subchH-part830.md)
- [Part 860 — Medical Device Classification Procedures](/cfr/21/chI-subchH-part860.md)
- [Part 861 — Procedures for Performance Standards Development](/cfr/21/chI-subchH-part861.md)
- [Part 862 — Clinical Chemistry and Clinical Toxicology Devices](/cfr/21/chI-subchH-part862.md)
- [Part 864 — Hematology and Pathology Devices](/cfr/21/chI-subchH-part864.md)
- [Part 866 — Immunology and Microbiology Devices](/cfr/21/chI-subchH-part866.md)
- [Part 868 — Anesthesiology Devices](/cfr/21/chI-subchH-part868.md)
- [Part 870 — Cardiovascular Devices](/cfr/21/chI-subchH-part870.md)
- [Part 872 — Dental Devices](/cfr/21/chI-subchH-part872.md)
- [Part 874 — Ear, Nose, and Throat Devices](/cfr/21/chI-subchH-part874.md)
- [Part 876 — Gastroenterology-Urology Devices](/cfr/21/chI-subchH-part876.md)
- [Part 878 — General and Plastic Surgery Devices](/cfr/21/chI-subchH-part878.md)
- [Part 880 — General Hospital and Personal Use Devices](/cfr/21/chI-subchH-part880.md)
- [Part 882 — Neurological Devices](/cfr/21/chI-subchH-part882.md)
- [Part 884 — Obstetrical and Gynecological Devices](/cfr/21/chI-subchH-part884.md)
- [Part 886 — Ophthalmic Devices](/cfr/21/chI-subchH-part886.md)
- [Part 888 — Orthopedic Devices](/cfr/21/chI-subchH-part888.md)
- [Part 890 — Physical Medicine Devices](/cfr/21/chI-subchH-part890.md)
- [Part 892 — Radiology Devices](/cfr/21/chI-subchH-part892.md)
- [Part 895 — Banned Devices](/cfr/21/chI-subchH-part895.md)
- [Part 898 — Performance Standard for Electrode Lead Wires and Patient Cables](/cfr/21/chI-subchH-part898.md)