510(k) K142567 ยท GWE Stimulator, Photic, Evoked Response
RETeval Visual Electrodiagnostic Device
| Applicant | Lkc Technologies, Inc., Gaithersburg MD, US |
| Decision | Substantially Equivalent, May 19, 2015 |
| Received | Sep 12, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142567
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.