510(k) K900997 ยท GXY Electrode, Cutaneous
K-STERILE TENS ELECTRODES
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Mar 13, 1990 |
| Received | Mar 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900997
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.