STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT

STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT is an FDA 510(k)-cleared medical device (K003577) manufactured by STERIS Corporation. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 28, 2001. Regulation: 8.