by
Brendon Nafziger, DOTmed News Associate Editor | March 22, 2011
i5 Nexus-DRF
(Courtesy InfiMed)
InfiMed Inc. said Tuesday its i5 Nexus-DRF digital imaging system received U.S. Food and Drug Administration 510(k) clearance.
The fifth-generation system is designed to reduce equipment costs by supporting RF, DR and cardiac capabilities on one console, according to materials posted on the Liverpool, N.Y.-based InfiMed's website.
Currently, it supports the Varian PaxScan 4030CB and Trixell Pixium RF 4343 dynamic flat panel detectors, with more to be added soon, the company said.
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The product includes InfiVision image-enhancement software.
InfiMed licenses its technology to resellers or OEMs. The Nexus-DRF is designed to be sold as a full system or a software package, the company said.
