AI-Powered Multi-Modal Cancer Risk Assessment | FDA 510(k) Compliant
Supported: CT, MRI, PET, X-Ray (DICOM format)
Based on comprehensive multi-modal AI analysis combining medical imaging and clinical data.
Schedule specialist consultation within 1-2 weeks
Recommend confirmatory imaging (CT/MRI/PET scan)
Follow-up imaging in 6 months to monitor progression
This AI-enabled medical device (Class II, FDA 510(k)) provides clinical decision support and does not replace professional medical judgment. All findings and recommendations must be reviewed and validated by a licensed healthcare provider before clinical application. This system is intended as an adjunct tool for healthcare professionals only.
For medical emergencies, call 911 (US) or your local emergency number immediately.