510(k) K172843 ยท KOI Stimulator, Nerve, Peripheral, Electric
TwitchView System
| Applicant | Blink Device Corporation, Seattle WA, US |
| Decision | Substantially Equivalent, Mar 29, 2018 |
| Received | Sep 19, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172843
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.