Cardiology
Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor
Verily Life Sciences LLC
FDA
FDA-cleared AI medical device
FDA Submission Metadata
- Submission number
- K213357
- Decision date
- July 2022
- FDA panel
- Cardiovascular
- Product code
- DXH
- Clinical task (npj)
- detection
- Data modality (npj)
- Signals
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.
Regulatory Approvals
FDA
US FDA 510k
K213357
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.