MODEL 430-07 ENDOCARDIAL PACING LEAD

MODEL 430-07 ENDOCARDIAL PACING LEAD is an FDA 510(k)-cleared medical device (K954610) 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 December 15, 1996. Regulation: 8.