510(k) K211974 ยท GWE Stimulator, Photic, Evoked Response
LED PHOTIC System
| Applicant | Micromed S.P.A., Mogliano Veneto, IT |
| Decision | Substantially Equivalent, Sep 23, 2021 |
| Received | Jun 25, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211974
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.