510(k) K832296 ยท GXY Electrode, Cutaneous
S2 POSTERIOR-TIB
| Applicant | Anstek Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 31, 1983 |
| Received | Jul 13, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832296
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.