7 devices · 2 companies · 2020 to 2026
Mim Software, Inc.: AI-enabled devices on FDA's list
7 devices from Mim Software, Inc., 2020 to 2026, from 2 companies across 1 product code. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (7 of 7 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 |
|---|---|---|---|---|
| Contour ProtégéAI+K253270 · 510(k) | Radiology | QKB | database entry | |
| Contour ProtégéAI+K250035 · 510(k) | Radiology | QKB | database entry | |
| Contour ProtégéAIK231765 · 510(k) | Radiology | QKB | database entry | |
| Contour ProtégéAIK223774 · 510(k) | Radiology | QKB | database entry | |
| Contour ProtégéAIK213976 · 510(k) | Radiology | QKB | database entry | |
| Contour ProtegeAIK210632 · 510(k) | Radiology | QKB | database entry | |
| Contour ProtegeAIK193252 · 510(k) | Radiology | QKB | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.