510(k) K210805 ยท GXY Electrode, Cutaneous
Ceribell Instant EEG Headband
| Applicant | Ceribell, Inc., Mountainview CA, US |
| Decision | Substantially Equivalent, Aug 30, 2021 |
| Received | Mar 17, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210805
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.