IMPLANT PACING LEAD TINED #3390, MODIFICATION

IMPLANT PACING LEAD TINED #3390, MODIFICATION is an FDA 510(k)-cleared medical device (K913203) 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.