PRODUCTS IMPLANT PACING LEAD, TINED, MODIFICATION

PRODUCTS IMPLANT PACING LEAD, TINED, MODIFICATION is an FDA 510(k)-cleared medical device (K913201) 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.