510(k) K192958 ยท KOI Stimulator, Nerve, Peripheral, Electric
TwitchView System
| Applicant | Blink Device Company, Seattle WA, US |
| Decision | Substantially Equivalent, Apr 2, 2020 |
| Received | Oct 22, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192958
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.