Cardiology
PreemptiveAI Clinical SDK
Measure Labs, Inc. (Dba Preemptiveai, Inc.)
FDA-cleared AI medical device
FDA Submission Metadata
- Submission number
- K250233
- Decision date
- February 2026
- FDA panel
- Cardiovascular
- Product code
- DXH
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.