KONICA LD-4500 LASER DIGITIZER

KONICA LD-4500 LASER DIGITIZER is an FDA 510(k)-cleared medical device (K933830) manufactured by Konica Medical 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 December 13, 1993. Regulation: 8.