510(k) K960732 ยท GXY Electrode, Cutaneous
HYDROSPOT EEG ELECTRODE MODEL 1501, HYDROSPOT LEADWIRE MODEL 1500
| Applicant | Physiometrix, Inc., N. Billerica MA, US |
| Decision | Substantially Equivalent, Apr 15, 1996 |
| Received | Feb 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960732
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.