FDA 510(k) Applications Submitted by STEFAN WALTER

FDA 510(k) Number Submission Date Device Name Applicant
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
K193352 12/04/2019 AbutmentCAD exocad GmbH
K183458 12/13/2018 exoplan 2.3 exocad GmbH


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