Philips receives FDA 510(k) clearance for its Rembra platform, expanding access to faster, more precise CT imaging across frontline care and cancer treatment planning
Philips receives FDA clearance for Rembra platform of scanning systems, including Rembra CT, Rembra RT and Areta RT, expanding access to faster, more precise imaging.
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Philips receives FDA 510(k) clearance for Smart Fit TorsoCardiac coil for 1.5T MR imaging, supporting patient comfort and streamlined workflows
Philips receives FDA 510(k) clearance for its Smart Fit TorsoCardiac 1.5T MR coil, designed to improve workflow efficiency and patient comfort.
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Philips receives FDA 510(k) clearance for its Rembra platform, expanding access to faster, more precise CT imaging across frontline care and cancer treatment planning
Philips receives FDA clearance for Rembra platform of scanning systems, including Rembra CT, Rembra RT and Areta RT, expanding access to faster, more precise imaging.
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Philips launches new Bridge Plus Occlusion Balloon to help manage rare but life-threatening SVC tears during lead extraction
Philips launches new Bridge Plus Occlusion Balloon to help manage rare but life-threatening SVC tears during lead extraction.
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Philips receives FDA 510(k) clearance for Verida, the world’s first AI-powered detector-based spectral CT*, advancing diagnostic precision across clinical applications
Philips receives FDA 510(k) clearance for Verida CT, bringing AI-powered spectral CT to the United States, advancing diagnostic precision.
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Why resilience in MRI now matters as much as performance
Resilience in healthcare can no longer be reactive. the ability to keep essential services running when disruption hits - and to restore them quickly when it does - must be designed in long before it’s needed.
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FDA clears Philips AI solution that provides real-time guidance during complex minimally invasive heart valve repair
FDA clears Philips AI solution that provides real-time guidance during complex minimally invasive heart valve repair.
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