K-DEFIB/PACE, MODEL KDP-60A

K-DEFIB/PACE, MODEL KDP-60A is an FDA 510(k)-cleared medical device (K002806) 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 November 20, 2000. Regulation: 8.