510(k) K002219 ยท GXY Electrode, Cutaneous
WANDY SELF-ADHESIVE NEUROSTIMULATION ELECTRODE
| Applicant | Wandy Rubber Industrial Co., Ltd., Shi-Chih, Taipei, TW |
| Decision | Substantially Equivalent, Feb 2, 2001 |
| Received | Jul 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002219
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.