Library / Laws / 115th Congress / House Bills / H.R. 2163
H.R. 2163
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.
| Print stage | Date | Size | ⠃ |
|---|---|---|---|
| Introduced in House | 2017-04-26 | 2.4K | ⠃⠗⠋ |