510(k) K854664 ยท IKT Electrode, Needle, Diagnostic Electromyograph
MEB-5200
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 14, 1986 |
| Received | Nov 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854664
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.