MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD

MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD is an FDA 510(k)-cleared medical device (K883265) manufactured by Telectronics and Cordis Pacing Systems. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on October 13, 1988. Regulation: 8.