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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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