Philips Launches Alturion Ultrasound System with FDA Clearance and AI-Powered Workflow
PHG•Philips received FDA 510(k) clearance and CE mark for its Alturion ultrasound system, launching in the US and Europe with a 24-inch monitor, responsive processing and AI-powered Elevate Plus measurements. The platform’s workflows automate measurements and share transducers with EPIQ Elite and Affiniti systems to streamline high-volume clinical exams.
1. Product Launch and Regulatory Approvals
Philips has introduced the Alturion ultrasound system following FDA 510(k) clearance and CE mark certification. The system is now available in the US and Europe, targeting high-volume clinical environments that demand rapid throughput without sacrificing image quality.
2. AI-Powered Workflow Features
Alturion includes Elevate Plus AI-driven measurement tools that automate acquisition and calculations for abdominal exams, reducing manual adjustments and exam time. These capabilities aim to enhance consistency across users by minimizing variability and supporting confident clinical decisions.
3. Hardware Design and Performance
Built on a powerful processing architecture, the system delivers responsive performance and clear visualization across diverse patient profiles. It features an expansive 24-inch monitor, a compact footprint for easy department-to-bedside mobility, and an intuitive interface to support operational simplicity.
4. Integration Within Connected Ecosystem
Alturion shares a common user interface and interchangeable transducers with Philips’ EPIQ Elite and Affiniti platforms, enabling streamlined training and departmental consistency. The system is compatible with Collaboration Live tele-ultrasound for remote support, consultation and training sessions.
