K-STIK DEFIBRILLATION PADS

K-STIK DEFIBRILLATION PADS is an FDA 510(k)-cleared medical device (K863899) 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 November 11, 1986. Regulation: 8.