510(k) K123843 ยท GWF Stimulator, Electrical, Evoked Response
NEUROEPG SYSTEM
| Applicant | Strohl Medical Technologies, Kittery ME, US |
| Decision | Substantially Equivalent, Jun 5, 2013 |
| Received | Dec 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123843
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.