PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T

PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T is an FDA 510(k)-cleared medical device (K854471) manufactured by Minnesota Laser Corp.. 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 12, 1986. Regulation: 8.