Medical Device Safety Act of 2008
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Medical Device Safety Act of 2008 - Amends the Federal Food, Drug, and Cosmetic Act to provide that provisions preempting state and local requirements for medical devices intended for human use shall not be construed to modify or otherwise affect any action for damages or the liability of any person under state law. Makes this Act effective as if it were included in the Medical Device Amendments of 1976 and applicable to any civil action pending or filed on or after the date of enactment of this Act.
Referred to the House Committee on Energy and Commerce.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 6381: Medical Device Safety Act of 2008. 110th Congress. Open America. https://openamerica.io/bill/110-HR-6381/
"H.R. 6381: Medical Device Safety Act of 2008." 110th Congress, 2026, Open America, https://openamerica.io/bill/110-HR-6381/.
H.R. 6381, 110th Cong. (2026), https://openamerica.io/bill/110-HR-6381/.
[H.R. 6381: Medical Device Safety Act of 2008](https://openamerica.io/bill/110-HR-6381/)