GREENSBORO, N.C., Feb. 23 /PRNewswire/ -- Neuisys Imaging System Solutions, LLC announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance of the NeuViz 16 Multi-Slice Computed Tomography (CT) System. The NeuViz 16 is developed by Philips Neusoft Medical Systems, a joint venture between Royal Philips Electronics of the Netherlands and Neusoft Corporation of China.
"The NeuViz 16 is a state-of-the-art CT system that provides superior performance for the price and provides the clinical benefits of routine, sub-millimeter resolution, volume imaging and low-dose protocols," said Kim Russell, Neuisys president and chief executive officer. "The NeuViz 16 packs a tremendous amount of technology into a very economical footprint and is the perfect solution for diagnostic imaging centers and community hospitals that plan to upgrade from older single or multi-slice CT systems to 16-slice CT as well as a wide array of specialist physician groups considering in-office CT including urologists, gastroenterologists, pulmonologists, surgeons, and oncologists."
source: PR Newswire
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment