Category Archives: FDAnews Device Daily Bulletin
If all goes as the wireless health industry plans, it can start introducing far more products that allow physicians to monitor patients with no wires attached.
This week San Antonio-based AirStrip Technologies announced that it was expanding its suite of mobile patient monitoring applications to enable physicians to more easily access information housed in various electronic health record systems via their mobile devices.
MAZOR Surgical Robotics announced that it has received Korean Food and Drug Administration (KFDA) approval for its Renaissance System, a new generation surgical robot.
The Global Harmonization Task Force’s (GHTF) Study Group 1 has modified its definition of a medical device and provided an explicit definition for the term in vitro diagnostic (IVD) medical device, according to a final document released May 16.
The House Appropriations Committee subcommittee that oversees FDA funding recommends fiscal 2013 appropriations that would slightly reduce agency spending. A full committee markup of the bill, as yet unnumbered, hasn’t been scheduled but is expected later in June.