---
kind: "unit"
title: "21"
title_heading: "Food and Drugs"
key: "chI/subchH/part822"
level: "part"
label: "Part 822"
heading: "Postmarket Surveillance"
release: "ecfr-current"
date: "2026-08-27"
url: "https://uscodex.org/cfr/21/chI-subchH-part822"
sections_count: 38
---

# Part 822 — Postmarket Surveillance

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

## Contents

- [Subpart A — General Provisions](/cfr/21/chI-subchH-part822-subpartA.md)
- [Subpart B — Notification](/cfr/21/chI-subchH-part822-subpartB.md)
- [Subpart C — Postmarket Surveillance Plan](/cfr/21/chI-subchH-part822-subpartC.md)
- [Subpart D — FDA Review and Action](/cfr/21/chI-subchH-part822-subpartD.md)
- [Subpart E — Responsibilities of Manufacturers](/cfr/21/chI-subchH-part822-subpartE.md)
- [Subpart F — Waivers and Exemptions](/cfr/21/chI-subchH-part822-subpartF.md)
- [Subpart G — Records and Reports](/cfr/21/chI-subchH-part822-subpartG.md)