Philips MR 7700 System Receives FDA 510(k) Clearance
Royal Philips announced it has received FDA 510(k) clearance for the company’s new high-performance MR 7700 3.0T MR system.
Royal Philips announced it has received FDA 510(k) clearance for the company’s new high-performance MR 7700 3.0T MR system.
This first regional hub is integrating data containing X-Ray, CT, and MRI images across 13 NHS trusts in the consortium.
Royal Philips and France’s Rennes University Hospital have inked a five-year deal to support diagnostic, interventional imaging as well as patient monitoring and management.
Handheld and portable ultrasound solutions have become valuable tools for clinicians treating COVID-19 patients.
Read MoreUltrasound devices are portable, so they can be brought to the patient rather than bringing the patient to different rooms in the hospital. Lessening patient movement also reduces patient exposure to other patients and healthcare professionals.
Read MoreThe new ultrasound system combines dedicated transducers, enhanced processing, and software tools optimized for pediatrics to help improve the experience of both young patients and staff.
Read MoreThe U.S. FDA has granted 510(k) clearance to Royal Philips’ DigitalDiagnost C90 digital radiography system. Designed to increase patient throughput and decrease the time to diagnosis, the Philips DigitalDiagnost C90 helps healthcare facilities streamline workflow.
Read MoreRoyal Philips announces the release of IntelliSpace Discovery 3.0—a comprehensive, open platform to enable the development and deployment of artificial intelligence assets in radiology. This technology is currently being showcased at the annual meeting of the Radiological Society of North America.
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