6000 ND:YAG LASER FOR BENIGN/MALIGNANT OBSTRUCTION

6000 ND:YAG LASER FOR BENIGN/MALIGNANT OBSTRUCTION is an FDA 510(k)-cleared medical device (K862698) manufactured by Cooper Lasersonics, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 1986. Regulation: 8.