MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY

MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY is an FDA 510(k)-cleared medical device (K000669) manufactured by Medivision Endoscopy. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 25, 2000. Regulation: 8.