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".

Organization

Country / Region

United States

License

Other (Public Domain)

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