CODEMASTER XL + XL W/SHOCK ADVISORY OPTION

CODEMASTER XL + XL W/SHOCK ADVISORY OPTION is an FDA 510(k)-cleared medical device (K954957) manufactured by Hewlett-Packard Co.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 6, 1996. Regulation: 8.