Search Tag: Echosens

IMAGING Management

2013 22 Apr

Echosens™ has announced that its FibroScan® device received 510(k) clearance from the U.S. Food and Drug Administration (FDA) on 5 April 2013 and is now ready to market its pioneering technology in the United States. Today, 1800 FibroScan® devices are used worldwide both in research and routine clinical practice. The United States of America is...Read more