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Agilent Technologies, Inc.
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HEARTSTREAM XL DEFIBRILLATOR/MONITOR, MODEL M4735A is an FDA 510(k)-cleared medical device (K001725) manufactured by Agilent Technologies, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 7, 2000. Regulation: 8.