KYOKKO UM SERIES INTENSIFYING SCREEN

KYOKKO UM SERIES INTENSIFYING SCREEN is an FDA 510(k)-cleared medical device (K942399) manufactured by Fujifilm Medical System U.S.A., Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 9, 1994. Regulation: 8.