MODEL 432-01 BIOPORE IMPLANTABLE PACING LEAD

MODEL 432-01 BIOPORE IMPLANTABLE PACING LEAD is an FDA 510(k)-cleared medical device (K862053) manufactured by Intermedics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 18, 1986. Regulation: 8.