510(k) K864660 ยท IKN Electromyograph, Diagnostic
MODEL M402 EMG MONITOR
| Applicant | Bio-Logic Devices, Deer Park NY, US |
| Decision | Substantially Equivalent, Feb 4, 1987 |
| Received | Nov 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864660
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.