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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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