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See Latest ArticlesNaviscan Receives 510(k) Clearance for Stereo Navigator - the First Commercially Available Breast PET-Guided Biopsy Feature
Corporate News Releases - The Healthcare Sales & Marketing Network, 11/20/08
Naviscan, Inc., announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its biopsy-guidance feature designed exclusively for use with its high-resolution organ-specific PET scanner. The scanner's breast application is Positron Emission Mammography (PEM).
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