Philips Image Guided Therapy Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 6
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253714 | IntraSight Plus | February 24, 2026 |
| K251103 | VeriSight Intracardiac Echocardiography Catheter (VSICE2D); VeriSight Pro Intracardiac Echocardiogra | May 9, 2025 |
| K200812 | VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter | September 2, 2020 |
| K200410 | Reconnaissance PV .018 OTW Digital IVUS Catheter | May 22, 2020 |