510(k) K984052 ยท IKN Electromyograph, Diagnostic
SYNERGY IOM SYSTEM
| Applicant | Oxford Instruments Medical Systems, Crofton MD, US |
| Decision | Substantially Equivalent, May 17, 1999 |
| Received | Nov 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984052
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.