SOPRO 225 DUAL HALOGEN LIGHT SOURCE

SOPRO 225 DUAL HALOGEN LIGHT SOURCE is an FDA 510(k)-cleared medical device (K072912) manufactured by Sopro. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 15, 2007. Regulation: 8.