
Physio-Control, Inc.
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LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR is an FDA 510(k)-cleared medical device (K130454) manufactured by Physio-Control, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on August 20, 2013. Regulation: 8.

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