510(k) K220161 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
Biofeedback Nerve and Muscle Stimulator
| Applicant | Shenzhen Konmed Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jul 20, 2022 |
| Received | Jan 20, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220161
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.