LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-

LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS- is an FDA 510(k)-cleared medical device (K850432) 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 February 14, 1985. Regulation: 8.