Informatics and digital radiography firm Viztek has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Exa PACS.
Exa PACS is Web-based and compatible with all devices and operating systems at hospitals, imaging centers, and teleradiology firms, Viztek said.
Exa features zero-footprint technology that allows the viewer to be operational within a Web browser, eliminating the need to install additional programs.
In addition, server-side rendering enables physicians to bypass the delays of prefetching or autorouting when opening large imaging studies, and it provides access from any location with diagnostic quality viewing.
