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SonoSite lands FDA 510(k) clearance for its 1st-of-its-kind X-Porte ultrasound kiosk, planning to launch U.S. commercial efforts immediately.

SonoSite wins 510(k) clearance for ultrasound kiosk

SonoSite this month won 510(k) clearance from the FDA to market its X-Porte ultrasound kiosk in the U.S., and the device maker's planning to start shipping the device immediately.

The Bothell, Wash.-based medical device company said called the kiosk is an "important milestone" in providing access to point-of-care ultrasound visualization. The kiosk uses SonoSite's proprietary Extreme Definition Imaging, which reduces imaging clutter to provide a higher resolution picture.

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