21 CFR Chapter I Subchapter H – Medical Devices – Part 822 Postmarket Surveillance
Information
Type
Regulation
Regulated products
Medical Devices
Last updated
June 4, 2024
Description
This document is a regulation titled "21 CFR Chapter I Subchapter H – Medical Devices – Part 822 Postmarket Surveillance".
Tags
Organization
Country / Region
United States
License
Other (Public Domain)