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Medtronic Emergency Response Systems, Inc.
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LIFEPAK 20 DEFIBRILLATOR/ MONITOR is an FDA 510(k)-cleared medical device (K063119) manufactured by Medtronic Emergency Response Systems, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 21, 2006. Regulation: 8.