2 devices · 1 company · 2022 to 2025
HeartLung Corporation: AI-enabled devices on FDA's list
2 devices from HeartLung Corporation, 2022 to 2025, from 1 company across 2 product codes. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (2 of 2 here), the regulation, and MAUDE report counts by product code.
Retrieved from FDA public records.
Product codes from HeartLung Corporation
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| AI-CVDK252029 · 510(k) | Radiology | QIH | database entry | |
| ABMD SoftwareK213760 · 510(k) | Radiology | KGI | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.