Philips Image Guided Therapy Corporation
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories4
Latest FDA decision2026-02-24
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253714 | IntraSight Plus | IYO | 2026-02-24 | View |
| PMA | P230021 | Stent, iliac vein | QAN | 2026-02-12 | View |
| 510(k) | K251103 | VeriSight Intracardiac Echocardiography Catheter (VSICE2D); VeriSight Pro Intracardiac Echocardiography Catheter (VSICE3D) | OBJ | 2025-05-09 | View |
| PMA | P180034 | Scaffold, dissection repair | QCT | 2022-09-29 | View |
| 510(k) | K200812 | VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter | OBJ | 2020-09-02 | View |
| 510(k) | K200410 | Reconnaissance PV .018 OTW Digital IVUS Catheter | OBJ | 2020-05-22 | View |
No matching devices.