To amend the Federal Food, Drug, and Cosmetic Act to require physicians and physician's offices to be treated as covered device users required to report on certain adverse events involving medical devices, and for other purposes.
Medical Device Guardians Act
This bill amends the Federal Food, Drug, and Cosmetic Act to require physicians to report significant adverse experiences caused by medical devices to the Food and Drug Administration.
Introduced in House
Introduced in House
Referred to the House Committee on Energy and Commerce.
Referred to the Subcommittee on Health.
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