510(k) K182022 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
ApexMV
| Applicant | Incontrol Medical, LLC, Brookfield WI, US |
| Decision | Unknown, Mar 15, 2019 |
| Received | Jul 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182022
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.