510(k) K862236 ยท IKN Electromyograph, Diagnostic
MYOLAB II, MODEL ML-200
| Applicant | Motion Control, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Aug 7, 1986 |
| Received | Jun 11, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862236
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.