510(k) K000870 ยท GXY Electrode, Cutaneous
KM-10 TENS ELECTRODE
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Nov 7, 2000 |
| Received | Mar 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000870
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.