510(k) K123399 ยท IKN Electromyograph, Diagnostic
MYOVISION 3.0 WIREFREE SYSTEM
| Applicant | Precision Biometrics, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Aug 1, 2013 |
| Received | Nov 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123399
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.