
Guidant Corporation, Cardiac Surgery
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VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 is an FDA 510(k)-cleared medical device (K022718) manufactured by Guidant Corporation, Cardiac Surgery. 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 August 27, 2002. Regulation: 8.