510(k) K003287 ยท KZM Device, Muscle Monitoring
MODEL K7 EVALUATION DEVICE
| Applicant | Myotronics-Noromed, Inc., Tukwila WA, US |
| Decision | Substantially Equivalent, Nov 6, 2000 |
| Received | Oct 20, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003287
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.