Women's Health Weekly
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Breast Cancer
U.S. FDA clears MammoReport(Plus) for extended use
March 24th, 2005
The U.S. Food and Drug Administration (FDA) has granted Siemens Medical Solutions 510(k) clearance for MammoReport(Plus), a mammography softcopy reporting workstation. The clearance allows for the processing of digital computer-aided (CAD) images and mammograms from approved vendors, expanded indications for multimodality viewing, and use with FDA-cleared monitors for the interpretation of lossless compressed images. In addition, MammoReport(Plus) is now Windows-based which enables it to run on syngo - the software platform from Siemens. The system's user-specific keypad and roaming/panning function allow for full spatial resolution and let users...
Source: Women's Health Weekly (2005-03-24)
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