MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASE

MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASE is an FDA 510(k)-cleared medical device (K880930) manufactured by Copper Lasersonics, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 30, 1988. Regulation: 8.