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.

USA115^th CongressHR-2163| House

| Updated: 5/5/2017

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.

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Health

Drug safety, medical device, and laboratory regulationHealth care qualityHealth information and medical recordsHealth personnelHealth technology, devices, suppliesProduct safety and quality

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.

USA115^th CongressHR-2163| House

| Updated: 5/5/2017

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Brian K. Fitzpatrick

Republican Representative

Pennsylvania

Cosponsors (2)

Rosa L. DeLauro (Democratic)Louise McIntosh Slaughter (Democratic)

Health Subcommittee, Energy and Commerce Committee

Health

Introduced
In Committee
On Floor
Passed Chamber
Enacted

Drug safety, medical device, and laboratory regulationHealth care qualityHealth information and medical recordsHealth personnelHealth technology, devices, suppliesProduct safety and quality

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.

Suggested Questions

Health

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.

Suggested Questions

Brian K. Fitzpatrick

Health Subcommittee, Energy and Commerce Committee

Health

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.

Suggested Questions

Health

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.

Suggested Questions

Brian K. Fitzpatrick

Health Subcommittee, Energy and Commerce Committee

Health