510(k) K243788 ยท GXY Electrode, Cutaneous
IceCap product line
| Applicant | Bioserenity Medical Devices Group, Paris, FR |
| Decision | Substantially Equivalent, Mar 13, 2025 |
| Received | Dec 9, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243788
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.