510(k) K000220 ยท IKN Electromyograph, Diagnostic
MA-300 ELECTROMYOGRAPHY SYSTEM
| Applicant | Motion Lab Systems, Inc., Baton Rouge LA, US |
| Decision | Substantially Equivalent, Feb 24, 2000 |
| Received | Jan 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000220
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.