GALILEO ENDOSCOPES

GALILEO ENDOSCOPES is an FDA 510(k)-cleared medical device (K962116) manufactured by Galileo Electro-Optics 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 November 26, 1996. Regulation: 8.