FUJI HG-M INTENSIFYING SCREEN

FUJI HG-M INTENSIFYING SCREEN is an FDA 510(k)-cleared medical device (K943425) 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 August 16, 1994. Regulation: 8.