510(k) K251936 ยท NCG Neuropsychiatric Interpretative Electroencephalograph Assessment Aid
Ceribell Delirium Monitor System
| Applicant | Ceribell, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Dec 8, 2025 |
| Received | Jun 24, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251936
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.