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Home » FDA Awards 510(k) Clearance to Visaris Portfolio

FDA Awards 510(k) Clearance to Visaris Portfolio

November 20, 2015

Visaris Americas has won FDA 510(k) clearance for its software, flat panel detectors and various hardware offerings.

The company’s Avanse technology is a system for the digital upgrade of radiography devices with the latest generation flat panel detectors. It enables facilities to smoothly transition to a single software platform, Visaris says.

Rick Sbordone, vice president digital sales and business development at Visaris, says Avanse supports several advanced imaging capabilities that are typically cost prohibitive in some market segments.

The company will launch its digital radiography solutions portfolio at the Radiological Society of North America conference in Chicago at the end of November. — Michael Cipriano

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