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Varian Medical Systems Receives FDA 510(k) Clearance of its Nexus DRF Digital X-Ray Imaging System
Date:5/22/2013

SALT LAKE CITY, May 22, 2013 /PRNewswire/ -- Varian Medical Systems (NYSE: VAR) today announced it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for Varian's diagnostic X-ray image processing workstation that combines radio frequency (RF) and digital radiography (DR) capabilities on one platform.  Varian's Nexus DRF Digital X-Ray Imaging System™ has the ability to interface with a variety of image receptors, including CCD cameras and commercially available flat-panel image detectors. 

"Nexus is Varian's 6th generation image processing platform," said Carl LaCasce vice president and general manager for Varian's Imaging Products business.  "It's an updated platform designed to provide our customers with a universal system that addresses both dynamic and static imaging modalities, as well as CCD camera based fluoroscopy.

The Nexus system enables an operator to acquire, display, process, transmit, export, or print high resolution X-ray images.  The advanced image processing algorithms make it possible to bring out diagnostic details that can be difficult to see using conventional imaging techniques.  The major system components include an image detector, a computer, a high resolution monitor, and Varian's proprietary image processing software.  Each system can be set up to process data from multiple receptors and detectors.

"By integrating both RF and DR capabilities on the Nexus console, we seek to provide our OEM partners with a standardized platform to optimize workflow and reduce time to market and equipment costs," adds LaCasce.  "Varian views its Nexus product as a cost effective, reliable solution to support a wide range of our customers' requirements." 

Nexus builds on Varian's current i5 line of digital
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SOURCE Varian Medical Systems
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