510(k) K911388 ยท IKN Electromyograph, Diagnostic
CAVOMAT
| Applicant | Wiest USA, Inc., Potomac MD, US |
| Decision | Substantially Equivalent, Dec 4, 1991 |
| Received | Mar 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911388
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.