510(k) K190617 ยท GXY Electrode, Cutaneous
Wrap accessory electrodes
| Applicant | Hi-Dow International, Inc., Maryland Heights MO, US |
| Decision | Substantially Equivalent, Jul 2, 2019 |
| Received | Mar 11, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190617
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.