510(k) K262515 ยท GYD Transducer, Tremor
Kneu Platform (V2)
| Applicant | Kneu Health Digital , Ltd., London, GB |
| Decision | Substantially Equivalent, Aug 20, 2026 |
| Received | Jul 21, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262515
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.