510(k) K142624 ยท GWF Stimulator, Electrical, Evoked Response
Neuromaster G1 MEE200
| Applicant | Nihon Kohden Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Apr 24, 2015 |
| Received | Sep 16, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142624
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.