510(k) K912643 ยท GXY Electrode, Cutaneous
ELECTRODE
| Applicant | Skylark Device Co., Ltd., Taipei, Taiwan, R.O.C., TW |
| Decision | Substantially Equivalent, Feb 14, 1992 |
| Received | Jun 14, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912643
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.