STRYKER ENDOSCOPIC INSTRUMENTS AND ACCESSORIES

STRYKER ENDOSCOPIC INSTRUMENTS AND ACCESSORIES is an FDA 510(k)-cleared medical device (K935237) manufactured by Stryker Endoscopy. 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 March 20, 1994. Regulation: 8.