MODEL 43100A SERIES DEFIBRILLATOR, MODIFICATION

MODEL 43100A SERIES DEFIBRILLATOR, MODIFICATION is an FDA 510(k)-cleared medical device (K910754) manufactured by Hewlett-Packard Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 7, 1991. Regulation: 8.