2 devices · 2 companies · 2023 to 2025
Feops NV: AI-enabled devices on FDA's list
2 devices from Feops NV, 2023 to 2025, from 2 companies 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 Feops NV
Panels
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| FEops HEARTguide Simulation ApplicationK250635 · 510(k) | Cardiovascular | QQI | database entry | |
| FEops HEARTguideTM, FEops HEARTguideTM ALPACAK223855 · 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.