510(k) K921919 ยท KZM Device, Muscle Monitoring
MS-100 MYO-SCANNER OR MS-100 EMG SCANNER
| Applicant | Myo-Tronics, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Jan 7, 1993 |
| Received | Apr 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921919
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.