510(k) K010590 ยท IKN Electromyograph, Diagnostic
NEUROPACK MICRO, MODEL MED-9100A SERIES
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Jun 28, 2001 |
| Received | Feb 27, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010590
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.