510(k) K081591 ยท GWE Stimulator, Photic, Evoked Response
NEUCODIA
| Applicant | Verisci Corporation, Raritan NJ, US |
| Decision | Substantially Equivalent, May 15, 2009 |
| Received | Jun 6, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081591
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.