About This 510(k) Submission
K211874 is an FDA 510(k) clearance for the G?nther Tulip Vena Cava Filter Set for Femoral Vein Approach, G?nther Tulip Vena Cava Filter Set for Jugular Vein Approach, G?nther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach, a Filter, Intravascular, Cardiovascular (Class II — Special Controls, product code DTK), submitted by William Cook Europe Aps (Bjaeverskov, DK). The FDA issued a Cleared decision on July 28, 2021, 41 days after receiving the submission on June 17, 2021. This device falls under the Cardiovascular review panel. Regulated under 21 CFR 870.3375.