K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85

K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85 is an FDA 510(k)-cleared medical device (K012404) manufactured by Katecho, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 11, 2001. Regulation: 8.