510(k) K123902 ยท IKN Electromyograph, Diagnostic
PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)
| Applicant | Oktx, LLC, Tulsa OK, US |
| Decision | Substantially Equivalent, Sep 13, 2013 |
| Received | Dec 18, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123902
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.