510(k) K962283 ยท GXY Electrode, Cutaneous
EEG ELECTRODES
| Applicant | Teca, Inc., Pleasantiville NY, US |
| Decision | Substantially Equivalent, Dec 16, 1996 |
| Received | Jun 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962283
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.