K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80

K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80 is an FDA 510(k)-cleared medical device (K993745) manufactured by Katecho, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on February 2, 2000. Regulation: 8.