The FDA has recently granted 510(k) clearance to Philips for a range of its devices to be used to manage COVID-19 patients in the U.S. The approved products include the Affiniti series, EPIQ series, Lumify, CX50, and Sparq system. These...
The FDA has announced approval and authorization of Caption Health‘s AI software, Caption Guidance, to analyze and assist with cardiac ultrasounds (echocardiography). Heart disease kills approximately one out of every four Americans each year according to the Center for Disease...
Register to receive a free U.S. Market Report Suite for Medical Imaging Devices – MedSuite report synopsis and brochure Hitachi Healthcare Americas demonstrated its latest technologies at ASE 2018 in Nashville, TN on June 23rd – 25th. Committed to delivering solutions that...
Register to receive a free U.S. Market Report Suite for Medical Imaging Devices – MedSuite report synopsis and brochure SuperSonic Imagine, a company specializing in ultrasound medical imaging, announced that the Aixplorer® and Aixplorer® Ultimate ultrasound diagnostic systems have received 510(k) clearance...