# Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment:  Guidance for Industry and Food and Drug Administration Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/testing-and-labeling-medical-devices-for-safety-in-the-magnetic-resonance-mr-environment-guidance-for-industry-and-food-and-drug-administration-staff/035607b0-0a83-4ff4-914b-df00d3a2038b

> FDA guidance document: Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment:  Guidance for Industry and Food and Drug Administration Staff. Issue date: October 10, 2023. Get complete insights and analysis.

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## Details

- Title: Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment:  Guidance for Industry and Food and Drug Administration Staff
- Communication Type: Guidance Document
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
- Issue Date: 2023-10-10
- Last Changed: 2023-10-10
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2019-D-2837">FDA-2019-D-2837</a>

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