FDA 510(k) Applications Submitted by C2 THERAPEUTICS

FDA 510(k) Number Submission Date Device Name Applicant
K131523 05/28/2013 CRYOBALLOON FOCAL ABLATION SYSTEM C2 THERAPEUTICS
K101825 07/01/2010 CRYOBALLOON ABLATION SYSTEM C2 THERAPEUTICS
K150083 01/15/2015 Sidecar External Working Channel C2 THERAPEUTICS


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