HR 7253 United States House · 117th Congress

Clarifying Remanufacturing to Protect Patient Safety Act of 2022

Summary
Clarifying Remanufacturing to Protect Patient Safety Act of 2022 This bill specifies that entities that remanufacture medical devices in a manner that could change the performance or safety specifications or the intended use of the device must register with the Food and Drug Administration as producers of medical devices and comply with related requirements.
Bill status in committee 1 of 4 stages cleared
Introduction
Mar 2022
Committee Review
Floor Vote
President
Introduced Mar 28, 2022 Last action Mar 29, 2022
Floor votes

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Full legislative history

Actions timeline

Total actions
3
Key actions
0
Committee
2
Mar 29, 2022
Committee
Referred to the Subcommittee on Health.
lower
Mar 28, 2022
Committee
Referred to the House Committee on Energy and Commerce.
lower
Mar 28, 2022
Introduced
Introduced in House
lower
1 primary · 3 co-sponsors

Sponsors