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FDA 510(k) Applications Submitted by MC3 Incorporated
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180151
01/19/2018
MC3 Jugular Dual Lumen Catheter
MC3 Incorporated
K191935
07/19/2019
Nautilus Smart ECMO Module
MC3 Incorporated
K182914
10/18/2018
MC3 Vascular Access Kit 21030
MC3 Incorporated
K171610
06/01/2017
MC3 QuickFlow Dual Lumen Catheter
MC3 Incorporated
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