To amend the Federal Food, Drug, and Cosmetic Act to authorize requiring the manufacturers of a covered device to disclose to a patient all patient-specific data that is recorded or transmitted by the device and accessible to the manufacturer, 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. Patient Device Data Access Act of 2025. H.R. 6117. 119th
Cong., 1st
sess., Introduced in House November 18, 2025. https://www.govinfo.gov/app/details/BILLS-119hr6117ih.
APA
Congress, House of Representatives (2025, November 18). Patient Device Data Access Act of 2025 (H.R. 6117 (IH)). Retrieved from https://www.govinfo.gov/app/details/BILLS-119hr6117ih.
MLA
United States, Congress, House of Representatives. Patient Device Data Access Act of 2025. U.S. Government Publishing Office, https://www.govinfo.gov/app/details/BILLS-119hr6117ih. 119th Congress, H.R. 6117, Introduced in House 18 Nov. 2025.
Bluebook
H.R.6117 - 119th Congress (2025-2026): Patient Device Data Access Act of 2025, H.R.6117, 119th Cong. (2025), https://www.govinfo.gov/app/details/BILLS-119hr6117ih.
