IMPLANT PACING LEAD, TINED #3262, MODIFICATION

IMPLANT PACING LEAD, TINED #3262, MODIFICATION is an FDA 510(k)-cleared medical device (K913202) 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.