510(k) K161202

C2 Cryoballoon Ablation System by C2 Therapeutics, Inc. — Product Code GEH

K161202 is an FDA 510(k) premarket notification submitted by C2 Therapeutics, Inc. for the device "C2 Cryoballoon Ablation System". The FDA issued a decision of Substantially Equivalent on January 5, 2017. The device falls under product code GEH (Unit, Cryosurgical, Accessories), a Class II device regulated under 21 CFR 878.4350. C2 Therapeutics, Inc. has at least 9 other 510(k) clearances on record.