FDANonrulemakingFDA-2019-D-2837

Who commented on this docket

Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment; Draft Guidance for Industry and Food and Drug Administration Staff; Availability

1 organizations filed 1 public comment on Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment; Draft Guidance for Industry and Food and Drug Administration Staff; Availability, at the Food and Drug Administration. The comment window closed 2462d ago.

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closed 2462d ago

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