ILLUMINATED MEDIASTINOSCOPE

ILLUMINATED MEDIASTINOSCOPE is an FDA 510(k)-cleared medical device (K141622) manufactured by Aegis Surgical, Ltd.. 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 January 8, 2015. Regulation: 8.