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HR 2474 115th Congress House

Medical Product Review Harmonization Act of 2017

Official title: To amend the Federal Food, Drug, and Cosmetic Act to provide an alternative standard for substantial equivalence determinations for devices, and for other purposes.

Introduced: May 16, 2017 See on congress.gov
Health Drug safety, medical device, and laboratory regulationHealth technology, devices, suppliesPublic participation and lobbying
This bill died when the 115th Congress ended
It never became law before the 115th Congress (2017–2018) adjourned, and bills don't carry over to the next Congress. It would have to be reintroduced. You can still save it for reference, but it won't receive updates.
 Everywhere this bill has been 3 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
May 19, 2017
Referred to the Subcommittee on Health.
May 16, 2017
Referred to the House Committee on Energy and Commerce.
May 16, 2017
Introduced in House
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 Latest action May 19, 2017

Referred to the Subcommittee on Health.

 Plain-English summary Congressional Research Service

Medical Product Review Harmonization Act of 2017

This bill amends the Federal Food, Drug, and Cosmetic Act to establish an alternative standard for demonstrating a device's substantial equivalence to a medical device that has already been approved by the Food and Drug Administration.

 Bill text 1 version

Source documents hosted by congress.gov.

 Committees of jurisdiction 2
Cite this page click to expand
APA
U.S. Congress. (2026). H.R. 2474: Medical Product Review Harmonization Act of 2017. 115th Congress. Open America. https://openamerica.io/bill/115-HR-2474/
MLA
"H.R. 2474: Medical Product Review Harmonization Act of 2017." 115th Congress, 2026, Open America, https://openamerica.io/bill/115-HR-2474/.
Bluebook (legal)
H.R. 2474, 115th Cong. (2026), https://openamerica.io/bill/115-HR-2474/.
Markdown link
[H.R. 2474: Medical Product Review Harmonization Act of 2017](https://openamerica.io/bill/115-HR-2474/)
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