MODEL MF..D & MX..D PACEMAKER LEADS

MODEL MF..D & MX..D PACEMAKER LEADS is an FDA 510(k)-cleared medical device (K823898) manufactured by Oscor, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on April 29, 1983. Regulation: 8.