510(k) K251381 ยท GXY Electrode, Cutaneous
Ceribell Instant EEG Headcap (Small: C251, Medium: C252)
| Applicant | Ceribell, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Oct 31, 2025 |
| Received | May 2, 2025 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K251381
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.