Kubtec's Xpert 20 gets FDA OK

Digital x-ray firm Kub Technologies (Kubtec) of Fairfield, CT, has received 510(k) premarket clearance from the U.S. Food and Drug Administration (FDA) for its Xpert 20 digital specimen radiography device.

With a footprint smaller than 11 x 12 inches, the Xpert 20 is designed for the biopsy suite to locate very small microcalcifications. It features automatic exposure control, autocalibration, automatic window leveling, and the ability to send multiple images with annotations to PACS.

The Xpert 20 is available in digital detectors sizes of 2 x 2 or 2 x 4 inches and has DICOM-compliant software.

Related Reading

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Kubtec signs specimen x-ray deal with Hologic, July 14, 2008

UMS and Kubtec to market Xpert Mobile, May 25, 2007

Kubtec lands U.K., NASA order, July 27, 2006

Kubtec to bring Xpert 80 to Yale, April 13, 2006

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