510(k) K830702 ยท IKN Electromyograph, Diagnostic
NICOLET EMG SATELLITE
| Applicant | Nicolet Biomedical Instruments, Walker MI, US |
| Decision | Substantially Equivalent, Jul 12, 1983 |
| Received | Mar 7, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830702
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.