PROTECTISCOPE CS COLONOSCOPE, NON-INTRAPULL

PROTECTISCOPE CS COLONOSCOPE, NON-INTRAPULL is an FDA 510(k)-cleared medical device (K081004) manufactured by Stryker GI. 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 May 1, 2008. Regulation: 8.