510(k) K881703 ยท HRX Arthroscope
3M CARPAL TUNNEL
| Applicant | 3M Company, Cottae Grove MN, US |
| Decision | Substantially Equivalent, Jul 25, 1988 |
| Received | Apr 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881703
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.