United States · Bill · HR
H.R. 7253 (117th)
Clarifying Remanufacturing to Protect Patient Safety Act of 2022
Introduced
28 March 2022
Last action
—
Status
Referred to the Subcommittee on Health.
Sponsors
—
Subjects
Discovery layer
Source updated
3 January 2025
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.
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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 · EN · 28 March 2022
Introduced in House (PDF)
Introduced in House · EN · 28 March 2022
Introduced in House
summary · EN · 28 March 2022
Sponsors
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Related records
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Sources
PoliticalRepo is an index and interpretation layer, not the authoritative legal source.
- Official source: https://www.congress.gov/bill/117th-congress/house-bill/7253
- Open data entity: https://api.congress.gov/v3/bill/117/hr/7253