QUIKPAGE ARRHYTHMIA REPORT GENERATOR

QUIKPAGE ARRHYTHMIA REPORT GENERATOR is an FDA 510(k)-cleared medical device (K841083) manufactured by Agilent Technologies. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 6, 1985. Regulation: 8.