510(k) K883781 ยท IKN Electromyograph, Diagnostic
NICOLET NEUROPORT/ACE SYSTEM
| Applicant | Nicolet Instrument Corp., Madison WI, US |
| Decision | Substantially Equivalent, Jun 5, 1989 |
| Received | Sep 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883781
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.