510(k) K020784

JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS by Jostra AG — Product Code DWF

K020784 is an FDA 510(k) premarket notification submitted by Jostra AG for the device "JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS". The FDA issued a decision of Substantially Equivalent on January 9, 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. Jostra AG has at least 10 other 510(k) clearances on record.