MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS

MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS is an FDA 510(k)-cleared medical device (K885175) manufactured by Possis Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on July 13, 1989. Regulation: 8.