ZOLL D-900 DEFIBRILLATOR

ZOLL D-900 DEFIBRILLATOR is an FDA 510(k)-cleared medical device (K913484) manufactured by Zmi Corp.. 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 15, 1991. Regulation: 8.