CORDIS HI-FLEX PERVENOUS BIPOLAR LEAD

CORDIS HI-FLEX PERVENOUS BIPOLAR LEAD is an FDA 510(k)-cleared medical device (K860846) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 25, 1986. Regulation: 8.