STRYKER L3 HYDROLERT

STRYKER L3 HYDROLERT is an FDA 510(k)-cleared medical device (K022248) manufactured by Stryker Endoscopy. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 5, 2002. Regulation: 8.