510(k) K880573 ยท IKN Electromyograph, Diagnostic
MODIFIED NICOLET VIKING SYSTEM
| Applicant | Nicolet Biomedical Instruments, Madison WI, US |
| Decision | Substantially Equivalent, Mar 22, 1988 |
| Received | Feb 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880573
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.