Vasoview 6 Harvesting Cannula, Models Vh-2000, Vh-2001 & Vh-2002

K022718 is the FDA 510(k) clearance record for VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002, a class II device, cleared for Guidant Corporation, Cardiac Surgery on 2002-08-28 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 8 510(k) clearances for Guidant Corporation, Cardiac Surgery, from 2002-02-20 to 2008-02-08. As of 2026-09-10, FDA records show no recalls naming K022718.