510(k) K992694 ยท KZM Device, Muscle Monitoring
MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I
| Applicant | Myotronics-Noromed, Inc., Tukwila WA, US |
| Decision | Substantially Equivalent, Sep 10, 1999 |
| Received | Aug 12, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992694
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.