INTERMEDICS 430-07 BIPOL IMPLANT ENDOCARD PAC LEAD

INTERMEDICS 430-07 BIPOL IMPLANT ENDOCARD PAC LEAD is an FDA 510(k)-cleared medical device (K902672) 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 February 28, 1991. Regulation: 8.