AFP 17 X 4 AUTOMATIC FILM PROCESSOR

AFP 17 X 4 AUTOMATIC FILM PROCESSOR is an FDA 510(k)-cleared medical device (K925885) manufactured by Afp Imaging Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 8, 1993. Regulation: 8.