FDA 510(k) Applications Submitted by Dirk Mucha

FDA 510(k) Number Submission Date Device Name Applicant
K160369 02/10/2016 GuideWire FIAGON GMBH
K160479 02/22/2016 PointerShell Universal, PointerShell LS FIAGON GMBH
K151156 05/01/2015 Fiagon Navigation System FIAGON GMBH
K141456 06/02/2014 THE FIAGON NAVIGATION - EXTENDED INSTRUMENT SET ENT, REGISTRATIONPOINTER, VENTERAPOINTER, GUIDEWIRE, POINTERSHELL FIAGON GMBH
K161940 07/14/2016 Guidewire 0.6 Single Use FIGON GMBH
K162176 08/03/2016 Fiagon Navigation System Fiagon GmbH
K163209 11/15/2016 Fiagon Navigation System FIAGON GMBH
K133573 11/20/2013 FIAGON NAVIGATION SYSTEM FIAGON GMBH
K163416 12/05/2016 Fiagon Navigation û PointerTube Straight and PointerTube Keat FIAGON GMBH


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