3 devices · 1 company · 2023 to 2025
Ceevra, Inc.: AI-enabled devices on FDA's list
3 devices from Ceevra, Inc., 2023 to 2025, from 1 company across 1 product code. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (3 of 3 here), the regulation, and MAUDE report counts by product code.
Retrieved from FDA public records.
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| Ceevra Reveal 3+K243933 · 510(k) | Radiology | QIH | database entry | |
| Ceevra Reveal 3+K233568 · 510(k) | Radiology | QIH | database entry | |
| Ceevra Reveal 3K222676 · 510(k) | Radiology | QIH | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.