OSCOR PERMANENT PACING LEAD RZ MODEL SERIES

OSCOR PERMANENT PACING LEAD RZ MODEL SERIES is an FDA 510(k)-cleared medical device (K003918) 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 May 21, 2001. Regulation: 8.