510(k) K250153 ยท GYD Transducer, Tremor
Neu Platform
| Applicant | Neuhealth Digital , Ltd., London, GB |
| Decision | Substantially Equivalent, Apr 25, 2025 |
| Received | Jan 21, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250153
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.