MODEL 4900 ND:YAG LASER FOR ENDOMETRIAL ABLATION

MODEL 4900 ND:YAG LASER FOR ENDOMETRIAL ABLATION is an FDA 510(k)-cleared medical device (K880173) manufactured by Cooper 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 March 23, 1988. Regulation: 8.