DEFIBRILLATOR ANALYZER, DELTA 1000

DEFIBRILLATOR ANALYZER, DELTA 1000 is an FDA 510(k)-cleared medical device (K961595) manufactured by Netech 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 October 28, 1996. Regulation: 8.