510(k) K260998 ยท OMB Automatic Event Detection Software For Full-Montage Electroencephalograph
Ceribell Neurology Review Software
| Applicant | Ceribell, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jun 24, 2026 |
| Received | Mar 26, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260998
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.