K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60

K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60 is an FDA 510(k)-cleared medical device (K981737) 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 December 8, 1998. Regulation: 8.