
Medtronic Vascular
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CARDIOBLATE MONOPOLAR PEN, 60813, CARDIOBLATE MONOPOLAR XL, 60814 is an FDA 510(k)-cleared medical device (K070288) manufactured by Medtronic Vascular. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 17, 2007. Regulation: 8.