To amend the Federal Food, Drug, and Cosmetic Act to ensure that a medical device is not marketed based on a determination that the device is substantially equivalent to a predicate device that has been recalled, corrected, or removed from the market because of an intrinsic flaw in technology or design that adversely affects safety, and for other purposes.
The bill’s titles are written by its sponsor.
Sponsor and status
Sponsor. Representative for Massachusetts's 7th congressional district. Democrat.
Last Updated: Jan 31, 2012
Length: 11 pages
112th Congress, 2011–2013
This bill was introduced on January 31, 2012, in a previous session of Congress, but was not enacted.
Jan 31, 2012
Bills and resolutions are referred to committees which debate the bill before possibly sending it on to the whole chamber.
H.R. 3847 (112th) was a bill in the United States Congress.
A bill must be passed by both the House and Senate in identical form and then be signed by the President to become law.
This bill was introduced in the 112th Congress, which met from Jan 5, 2011 to Jan 3, 2013. Legislation not enacted by the end of a Congress is cleared from the books.
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GovTrack.us. (2020). H.R. 3847 — 112th Congress: Safety Of Untested and New Devices Act of 2012. Retrieved from https://www.govtrack.us/congress/bills/112/hr3847
“H.R. 3847 — 112th Congress: Safety Of Untested and New Devices Act of 2012.” www.GovTrack.us. 2012. February 19, 2020 <https://www.govtrack.us/congress/bills/112/hr3847>
Safety Of Untested and New Devices Act of 2012, H.R. 3847, 112th Cong..
|title=H.R. 3847 (112th)
|accessdate=February 19, 2020
|author=112th Congress (2012)
|date=January 31, 2012
|quote=Safety Of Untested and New Devices Act of 2012
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