Ceribell, Inc.
Ceribell, Inc. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2026.
Top product codes for Ceribell, Inc.
Recent clearances by Ceribell, Inc.
- K261101 — Ceribell Monitor
- K260998 — Ceribell Neurology Review Software
- K260363 — Ceribell Brain Monitor Headband
- K254033 — Ceribell Instant EEG Headset
- K251936 — Ceribell Delirium Monitor System
- K252070 — Ceribell Infant Seizure Detection Software
- K251381 — Ceribell Instant EEG Headcap (Small: C251, Medium: C252)
- K241589 — Ceribell Seizure Detection Software
- K232052 — Ceribell Instant EEG Headband
- K223504 — Ceribell Status Epilepticus Monitor
- K223086 — Ceribell Instant EEG Headcap
- K210805 — Ceribell Instant EEG Headband
- K191301 — Ceribell Pocket EEG Device
- K171459 — Ceribell Instant EEG Headband
- K170363 — Ceribell Pocket EEG Device
Data sourced from openFDA. This site is unofficial and independent of the FDA.