510(k) K131094 ยท IKN Electromyograph, Diagnostic
VIMOVE
| Applicant | Dorsa VI Pty., Ltd., Chalotte NC, US |
| Decision | Substantially Equivalent, Jul 11, 2014 |
| Received | Apr 18, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131094
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.