FDA 510(k) Applications Submitted by Johannes Messow

FDA 510(k) Number Submission Date Device Name Applicant
K180308 02/02/2018 Prelude MedCom GmbH
K170841 03/21/2017 BiopSee, Mobile US MedCom GmbH
K181789 07/05/2018 VeriSuite MedCom GmbH
K163119 11/08/2016 NaviSuite SSI Edition MEDCOM GMBH


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