2 devices · 1 company · 2021
Philips Medical Systems: AI-enabled devices on FDA's list
2 devices from Philips Medical Systems, 2021, 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 (2 of 2 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 |
|---|---|---|---|---|
| Philips EPIQ Diagnostic Ultrasound System, PhiliK212704 · 510(k) | Radiology | IYN | database entry | |
| EPIQ Series Diagnostic Ultrasound System, AffiniK211597 · 510(k) | Radiology | IYN | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.