
Medtronic Vascular
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MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626 is an FDA 510(k)-cleared medical device (K022238) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 8, 2002. Regulation: 8.

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