510(k) K944134 ยท KZM Device, Muscle Monitoring
K6-1 DIAGNOSTIC SYSTEM VERSION 3.1
| Applicant | Myo-Tronics, Inc., Tukwila WA, US |
| Decision | Substantially Equivalent, Dec 9, 1994 |
| Received | Aug 24, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944134
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.