Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment: Guidance for Industry and Food and Drug Administration Staff
Information
Type
Guidance
Regulated products
Medical Devices, Radiation-Emitting Products
Topics
Labeling, Premarket, Safety - Issues, Errors, And Problems
Published
October 10, 2023
Last updated
October 10, 2023
Description
A guidance document on testing and labeling medical devices for safety in the magnetic resonance environment.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)