SenoRx Inc. announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its SenoSonix System, an integration of its EnCor breast biopsy system with a state-of-the-art ultrasound Imaging system, incorporating SenoRx's EnCor vacuum-assisted biopsy technologies with an ultrasound system developed and sold by Ultrasonix Medical Corporation of Canada.
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