510(k) K000963 ยท GWF Stimulator, Electrical, Evoked Response
DA VINCHI EEG AND EMG/EP SYSTEMS
| Applicant | Airsep Corp., Buffalo NY, US |
| Decision | Substantially Equivalent, Oct 20, 2000 |
| Received | Mar 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000963
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.