To amend the Federal Food, Drug, and Cosmetic Act to require physicians and physician’s offices to be treated as covered device users required to report on certain adverse events involving medical devices, and for other purposes.
Citations are generated automatically from bibliographic data as a convenience and may not be complete or accurate.
Chicago
U.S. Congress. House. Medical Device Guardians Act of 2016. H.R. 5404. 114th
Cong., 2nd
sess., Introduced in House June 8, 2016. https://www.govinfo.gov/app/details/BILLS-114hr5404ih.
APA
Congress, House of Representatives (2016, June 8). Medical Device Guardians Act of 2016 (H.R. 5404 (IH)). Retrieved from https://www.govinfo.gov/app/details/BILLS-114hr5404ih.
MLA
United States, Congress, House of Representatives. Medical Device Guardians Act of 2016. U.S. Government Publishing Office, https://www.govinfo.gov/app/details/BILLS-114hr5404ih. 114th Congress, H.R. 5404, Introduced in House 8 Jun. 2016.
Bluebook
H.R.5404 - 114th Congress (2015-2016): Medical Device Guardians Act of 2016, H.R.5404, 114th Cong. (2016), https://www.govinfo.gov/app/details/BILLS-114hr5404ih.
