MULTILINE; DLY-1

MULTILINE; DLY-1 is an FDA 510(k)-cleared medical device (K930793) 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 August 18, 1993. Regulation: 8.