AII-PRO 100 PLUS AND ALL-PRO 200

AII-PRO 100 PLUS AND ALL-PRO 200 is an FDA 510(k)-cleared medical device (K991435) manufactured by All-Pro 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 May 19, 1999. Regulation: 8.