510(k) K203158 ยท GXY Electrode, Cutaneous
BioWave BioWraps
| Applicant | Biowave Corporation, Norwalk CT, US |
| Decision | Substantially Equivalent, Jul 8, 2021 |
| Received | Oct 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203158
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.