S.L.T. CONTACT LASER ND:YAG USE IN PULMONARY AIRWA

S.L.T. CONTACT LASER ND:YAG USE IN PULMONARY AIRWA is an FDA 510(k)-cleared medical device (K855095) manufactured by Surgical Laser Technologies, 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 February 17, 1986. Regulation: 8.