510(k) K864641 ยท IKN Electromyograph, Diagnostic
VENTEX-IA
| Applicant | Ventech Corp., Philadelphia PA, US |
| Decision | Substantially Equivalent, Jan 28, 1987 |
| Received | Nov 26, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864641
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.