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Padpro, LLC
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PADPRO MODEL 2001, 2001-S, 2001-C, 2001-EPS is an FDA 510(k)-cleared medical device (K014209) manufactured by Padpro, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on January 17, 2002. Regulation: 8.