El Nexo-DRF de InfiMed i5 consigue la AUTORIZACIÓN del FDA
por Brendon Nafziger, DOTmed News Associate Editor | March 22, 2011
i5 Nexus-DRF
(Courtesy InfiMed)
(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.
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.
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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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.
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