510(k) K113677 ยท KZM Device, Muscle Monitoring
GRINDCARE MEASURE
| Applicant | Medotech A/S, Westminster CO, US |
| Decision | Substantially Equivalent, Apr 5, 2012 |
| Received | Dec 14, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113677
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.