510(k) K232052 ยท GXY Electrode, Cutaneous
Ceribell Instant EEG Headband
| Applicant | Ceribell, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Aug 8, 2023 |
| Received | Jul 10, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232052
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.