OSCOR MEDICAL FIX SCREW PAC LEAD/PEEL CATH, MODIF

OSCOR MEDICAL FIX SCREW PAC LEAD/PEEL CATH, MODIF is an FDA 510(k)-cleared medical device (K913205) 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 September 22, 1991. Regulation: 8.