K251936
- 510(k) number
- K251936
- Device name
- Ceribell Delirium Monitor System
- Applicant
- Ceribell, Inc. CA · US
- Product code
- NCG — Neuropsychiatric Interpretative Electroencephalograp
- Decision date
- 2025-12-08
- Date received
- 2025-06-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251936.pdf
Official FDA record: K251936
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.