Philips Image Guided Therapy Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Image Guided Therapy Corporation - FDA 510(k) Cleared Devices
Recent clearances: IntraSight Plus, VeriSight Intracardiac Echocardiography Catheter (VSICE2D), VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter
4
Total
4
Cleared
0
Denied
Philips Image Guided Therapy Corporation has 4 FDA 510(k) cleared medical devices. Based in Colorado Springs, US.
Latest FDA clearance: Feb 2026. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Philips Image Guided Therapy Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Philips Ultrasound, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Philips Image Guided Therapy Corporation
4 devices
Cleared
Feb 24, 2026
IntraSight Plus
Cardiovascular
92d
Cleared
May 09, 2025
VeriSight Intracardiac Echocardiography Catheter (VSICE2D)
Cardiovascular
28d
Cleared
Sep 02, 2020
VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE...
Cardiovascular
159d
Cleared
May 22, 2020
Reconnaissance PV .018 OTW Digital IVUS Catheter
Cardiovascular
93d