510(k) K101763 ยท GWE Stimulator, Photic, Evoked Response
DIOPSYS NOVA VEP VISION TESTING SYSTEM
| Applicant | Diopsys, Inc., Pine Brook NJ, US |
| Decision | Substantially Equivalent, May 9, 2011 |
| Received | Jun 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101763
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.