510(k) K022272

MALLEABLE SINGLE STAGE VENOUS CANNULA, MODELS 68112-68140 (15 TOTAL CODES) by Medtronic Cardiac Surgical Products — Product Code DWF

K022272 is an FDA 510(k) premarket notification submitted by Medtronic Cardiac Surgical Products for the device "MALLEABLE SINGLE STAGE VENOUS CANNULA, MODELS 68112-68140 (15 TOTAL CODES)". The FDA issued a decision of Substantially Equivalent on January 8, 2003. The device falls under product code DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4210. Medtronic Cardiac Surgical Products has at least 6 other 510(k) clearances on record.