510(k) K862092 ยท KZM Device, Muscle Monitoring
COMFORTRON
| Applicant | M. D. Supply, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Oct 15, 1986 |
| Received | Jun 2, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862092
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.