Healthcare information systems firm Cerner of Kansas City, MO, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its ProVision mammography workstation.
ProVision is now available in North America and is designed to eliminate the need for separate viewers for general imaging and mammography. Radiologists can view all imaging modalities, including MRI, PET, ultrasound, CT, and x-ray, and a patient's electronic health record from one workstation.
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