510(k) K840108 ยท KOI Stimulator, Nerve, Peripheral, Electric
NEUROMUSCULAR TRANSMISSION MONITOR
| Applicant | Datex Division Instrumentarium Corp., Walker MI, US |
| Decision | Substantially Equivalent, Feb 17, 1984 |
| Received | Jan 10, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840108
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.