21 CFR Chapter I Subchapter H – Medical Devices – Part 810 Medical Device Recall Authority
Information
Type
Regulation
Regulated products
Medical Devices
Last updated
March 31, 2023
Description
This document is a regulation titled "21 CFR Chapter I Subchapter H – Medical Devices – Part 810 Medical Device Recall Authority".
Tags
Organization
Country / Region
United States
License
Other (Public Domain)