MARQUETTE SERIES 360 DEFIBRILLATOR

MARQUETTE SERIES 360 DEFIBRILLATOR is an FDA 510(k)-cleared medical device (K921487) manufactured by Marquette Electronics, 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 December 28, 1992. Regulation: 8.