510(k) K142369 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
Urinary Incontinence System
| Applicant | Guangzhou Finecure Medical Equipment Co.,Ltd, Guangzhou, CN |
| Decision | Substantially Equivalent, Jun 17, 2015 |
| Received | Aug 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142369
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.