Ultrasound developer Fujifilm SonoSite has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its iViz portable ultrasound device.
Designed for point-of-care settings, iViz features a 7-inch touchscreen display, as well as Fuji's SonoHD2 and SonoAdapt tissue optimization technology. It integrates ultrasound with hospital IT and electronic medical record systems and supports M-Mode and color velocity Doppler techniques, the company said.
Fujifilm SonoSite received the European CE Mark for iViz in September.