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Zdrowie i gospodarka · 20/05/2021

FDA Releases Final Guidance on Medical Device Testing for Magnetic Resonance Environment

The Food and Drug Administration (FDA) has made available a final guidance document outlining the testing and labeling requirements for medical devices in the Magnetic Resonance (MR) environment, aiming to enhance consistency in reviews and safety labeling across various medical devices.

Source: Federal Register — Food and Drug AdministrationOpen original release →