FDA 510(k) Applications Submitted by CARDIOGARD MEDICAL LTD

FDA 510(k) Number Submission Date Device Name Applicant
K182302 08/24/2018 CardioGard Emboli Protection Cannula CardioGard Medical Ltd
K141465 06/03/2014 CARDIOGARD EMBOLI PROTECTION CANNULA CARDIOGARD MEDICAL LTD


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