# Philips Image Guided Therapy Corporation

- Location (FDA's records): San Diego, CA
- FDA decisions: 6 (2019–2026): 4 510(k) clearances and 2 original PMA approvals
- Product codes: OBJ (3), QCT (1), QAN (1), IYO (1)
- 510(k) review time since 2016: median 93 days, against 135 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 2 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Volcano Corporation: 4 (https://510kreport.com/company/volcano)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)

## Firms that cite its devices most
- Provisio Medical, Inc.: 1 (https://510kreport.com/company/provisio-medical)

## Its most-cited devices
- K200812: VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter (2020), cited by 1
- K200410: Reconnaissance PV .018 OTW Digital IVUS Catheter (2020), cited by 1

## Recent decisions
- K253714: IntraSight Plus (Feb 24, 2026)
- K251103: VeriSight Intracardiac Echocardiography Catheter (VSICE2D); VeriSight Pro Intracardiac Echocardiography Catheter (VSICE3D) (May 9, 2025)
- P230021: Duo Venous Stent System (Dec 26, 2023)
- K200812: VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter (Sep 2, 2020)
- K200410: Reconnaissance PV .018 OTW Digital IVUS Catheter (May 22, 2020)
- P180034: Tack Endovascular System (6F) (Apr 11, 2019)

Source page: https://510kreport.com/company/philips-image-guided-therapy