510(k) K951118 ยท GEY Motor, Surgical Instrument, Ac-Powered
3M MAXI-DRIVER II ELECTRIC SYSTEM
| Applicant | 3M Company, Burbank CA, US |
| Decision | Substantially Equivalent, Jul 6, 1995 |
| Received | Mar 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951118
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.