ND:YAG LASER 4000/6000/8000 ENDOMETRIAL ABLATION

ND:YAG LASER 4000/6000/8000 ENDOMETRIAL ABLATION is an FDA 510(k)-cleared medical device (K862456) 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 August 11, 1986. Regulation: 8.