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Naviscan, a developer and marketer of high-resolution positron emission tomography scanners, has received the FDA 510(k) clearance for Stereo Navigator, its biopsy-guidance feature designed exclusively for use with its high-resolution organ-specific positron emission tomography scanner. The scanners breast application is positron emission mammography.
Naviscan, Inc., announced today that the U.S. Food and Drug Administration has granted 510 clearance for its biopsy-guidance feature designed exclusively for use with its high-resolution organ-specific PET scanner.
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