2 devices · 1 company · 2023 to 2025
Ceribell, Inc.: AI-enabled devices on FDA's list
2 devices from Ceribell, Inc., 2023 to 2025, from 1 company across 2 product codes. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (2 of 2 here), the regulation, and MAUDE report counts by product code.
Retrieved from FDA public records.
Product codes from Ceribell, Inc.
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| Ceribell Delirium Monitor SystemK251936 · 510(k) | Neurology | NCG | database entry | |
| Ceribell Status Epilepticus MonitorK223504 · 510(k) | Neurology | OMB | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.