510(k) DEN220073 ยท QXM Implanted Tibial Electrical Urinary Continence Device
Revi System
| Applicant | Bluewind Medical , Ltd., Herzliya, IL |
| Decision | Unknown, Aug 16, 2023 |
| Received | Oct 5, 2022 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN220073
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.