510(k) K172220

Advanced Perfusion System 1 by Terumo Cardiovascular Systems Corporation — Product Code DTQ

K172220 is an FDA 510(k) premarket notification submitted by Terumo Cardiovascular Systems Corporation for the device "Advanced Perfusion System 1". The FDA issued a decision of Substantially Equivalent on August 17, 2017. The device falls under product code DTQ (Console, Heart-Lung Machine, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4220. Terumo Cardiovascular Systems Corporation has at least 10 other 510(k) clearances on record.