DERMA-LASE RUBY LASER - MODEL DLR-1

DERMA-LASE RUBY LASER - MODEL DLR-1 is an FDA 510(k)-cleared medical device (K913256) manufactured by Derma-Lase Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 21, 1992. Regulation: 8.