- All Devices
- Radiology
- ART-Plan (v.2.2.0)
Radiology
ART-Plan (v.2.2.0)
Therapanacea SAS
FDA-cleared AI medical device
FDA Submission Metadata
- Submission number
- K234068
- Decision date
- April 2024
- FDA panel
- Radiology
- Product code
- MUJ
- Clinical task (npj)
- quantification/feature localization|synthetic data generation
- Data modality (npj)
- Images
This entry is sourced from the FDA AI/ML-Enabled Medical Devices list. No editorial review yet — the catalogue may add a deeper review of this device in future.
This entry is on our editorial review queue. Full evaluation — performance metrics, clinical evidence, safety record — lands as our review pipeline graduates each device. The information above is what's been verified to date.