Published in Medical Letter on the CDC and FDA, October 3rd, 2004
The FDA 510k approval denotes that the Coronis 5MP Mammo product, integrating several cutting-edge technologies to refine clinical diagnosis and increase productivity, has been officially cleared for use in digital mammography applications by the U.S. Food and Drug Administration (FDA).
The clearance came only a few weeks after the FDA's approval for Barcos CRT-based MGD 521M mammography display and marks the company's front-running position as a provider of innovative imaging technology in the field of mammography and Picture...
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