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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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