510(k) K171430 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
Incontinence Treatment Device, Model LT2061
| Applicant | Shenzhen Dongdixin Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Mar 15, 2018 |
| Received | May 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171430
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.