510(k) K923803 ยท GYC Electrode, Cortical
AD-TECH SUB DURAL ELECTRODEDS
| Applicant | Ad-Tech Medical Instrument Corp, Racine WI, US |
| Decision | Substantially Equivalent, Oct 23, 1992 |
| Received | Jul 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923803
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.