United States · Bill · HR
H.R. 2915 (116th)
Medical Device Guardians Act
Introduced
22 May 2019
Last action
—
Status
Referred to the Subcommittee on Health.
Sponsors
—
Subjects
Discovery layer
Source updated
3 January 2025
Summary
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.
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Votes
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Versions
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Documents
3 official files
Introduced in House (text)
Introduced in House (text)
Introduced in House · EN · 22 May 2019
Introduced in House (PDF)
Introduced in House · EN · 22 May 2019
Introduced in House
summary · EN · 22 May 2019
Sponsors
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Related records
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Sources
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- Official source: https://www.congress.gov/bill/116th-congress/house-bill/2915
- Open data entity: https://api.congress.gov/v3/bill/116/hr/2915