510(k) K912071 ยท IKN Electromyograph, Diagnostic
SPACE(TM) 7500
| Applicant | F.M. Wiest USA, Inc., Oradell NJ, US |
| Decision | Substantially Equivalent, Jul 9, 1991 |
| Received | May 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912071
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.