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Medtronic Physio-Control Corp.
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LIFEPAK 12, 20, 500, CR PLUS is an FDA 510(k)-cleared medical device (K033275) manufactured by Medtronic Physio-Control Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on November 5, 2003. Regulation: 8.