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H.R. 2915 · 116th Congress

Medical Device Guardians Act

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IntroducedPassed one chamberPassed both chambersBecame law (gold)Resolution agreed to (full, dark)Failed or vetoed (gray)

Under the number: the Yea · Nay count of its final (or latest) recorded vote. On a member's page, the small badge is how that member voted: Y Yea / Aye, N Nay / No, P Present, – Not voting.

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Never voted on. It didn't reach a floor vote before the 116th Congress ended, so it expired. A bill has to be introduced again to be considered in a new Congress.

3 cosponsors · 3 D

3 signed on when it was introduced; the rest joined later. Cosponsors who withdrew aren't shown.

This bill requires physicians to report significant adverse experiences caused by medical devices to the Food and Drug Administration (FDA).

What it does: CRS summary · Introduced in House · May 22, 2019

Medical Device Guardians Act

This bill requires physicians to report significant adverse experiences caused by medical devices to the Food and Drug Administration (FDA).

The FDA must establish an electronic reporting system to facilitate compliance with this bill and must publish the reports online.

Written by the nonpartisan Congressional Research Service. All summary versions on Congress.gov

About this bill and sources

Official title: Medical Device Guardians Act

Latest action (May 23, 2019): Referred to the Subcommittee on Health.

Policy area: Health · Origin: House · Introduced: May 22, 2019

Official page on Congress.gov · Bill text (GovInfo) · Status record (XML)

No recorded floor vote found.