FDA 510(k) Applications Submitted by MedCom GmbH

FDA 510(k) Number Submission Date Device Name Applicant
K022219 07/09/2002 EXOMIO, MODEL 1.1 MEDCOM GMBH
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
K133914 12/23/2013 VERISUITE 1.8, VERISUITE-PARTICLE 1.8, VERISUITE, VERISUITE-PARTICLE MEDCOM GMBH
K100056 01/08/2010 MEDCOM RT-VIEWER SYSTEM MEDCOM GMBH
K080742 03/17/2008 VERISUITE 1.6, VERISUITE-PARTICLE 1.6 MEDCOM GMBH
K102237 08/09/2010 PVS MODEL 1.0 MEDCOM GMBH
K032550 08/18/2003 EXOMIO, MODEL 2.0 SP1 MEDCOM GMBH
K092653 08/28/2009 VERISUITE AND VERISUITE-PARTICLE, VERSION 1.8 MEDCOM GMBH


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