FUJI MEDICAL DRY IMAGER FM-DP 2636

FUJI MEDICAL DRY IMAGER FM-DP 2636 is an FDA 510(k)-cleared medical device (K962967) manufactured by Fujifilm Medical System U.S.A., Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 27, 1996. Regulation: 8.