VASOVIEW HEMOPRO 2 ENDOSCOPIC VESSEL HARVESTING SYSTEM

VASOVIEW HEMOPRO 2 ENDOSCOPIC VESSEL HARVESTING SYSTEM is an FDA 510(k)-cleared medical device (K101274) manufactured by Maquet Cardiovascular, LLC. 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 10, 2010. Regulation: 8.