OSCOR MEDICAL CORP PERMANENT PACING LEAD

OSCOR MEDICAL CORP PERMANENT PACING LEAD is an FDA 510(k)-cleared medical device (K912867) manufactured by Oscor Medical Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on February 3, 1992. Regulation: 8.