Philips Granted FDA Clearance for Ultrasound Devices to Manage COVID-19 Complications

26/05/2020 iData Research

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, L... Read More

FDA Approves AI Software to Capture Heart Images Via Ultrasound

12/02/2020 iData Research

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 approxi... Read More

Hitachi Healthcare Americas Unveiled the Latest in Cardiovascular Ultrasound and Reporting at ASE 2018

09/07/2018 iData Research

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... Read More

Aixplorer® and Aixplorer® Ultimate Ultrasound Diagnostic Systems Receive 510(k) Clearance

15/02/2018 iData Research

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, an... Read More