510(k) K010543 ยท GXY Electrode, Cutaneous
KM-30 TENS ELECTRODE
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, May 23, 2001 |
| Received | Feb 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010543
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.