3 devices · 1 company · 2019 to 2022
Verily Life Sciences LLC: AI-enabled devices on FDA's list
3 devices from Verily Life Sciences LLC, 2019 to 2022, from 1 company across 1 product code. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (3 of 3 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 |
|---|---|---|---|---|
| Study Watch with Irregular Pulse MonitorK213357 · 510(k) | Cardiovascular | DXH | database entry | |
| Study Watch with Irregular Pulse MonitorK192415 · 510(k) | Cardiovascular | DXH | database entry | |
| Study WatchK182456 · 510(k) | Cardiovascular | DXH | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.