MODEL 329T PROGRAMMABLE, BIPOLAR CARDI

MODEL 329T PROGRAMMABLE, BIPOLAR CARDI is an FDA 510(k)-cleared medical device (K832893) manufactured by Cook Pacemaker Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on October 3, 1983. Regulation: 8.