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Zoll Medical Corporation, World Wide Headquarters
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ZOLL E SERIES 12SL, ANALYSIS OPTION is an FDA 510(k)-cleared medical device (K080232) manufactured by Zoll Medical Corporation, World Wide Headquarters. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on April 22, 2008. Regulation: 8.