FDA 510(k) Applications Submitted by OEHM UND REHBEIN GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K091364 05/08/2009 DICOMPACS, MODEL 5.2, DICOMPACS DX-R, MODEL 1.4 OEHM UND REHBEIN GMBH
K141440 06/02/2014 DICOMPACS DX-R WITH FLAT PANEL OEHM UND REHBEIN GMBH
K131211 04/29/2013 DICOMPACS DX-R WITH FLAT PANEL OEHM UND REHBEIN GMBH
K070618 03/05/2007 DICOMPACS, MODEL 5 OEHM UND REHBEIN GMBH
K182317 08/27/2018 AMADEO M-DR mini, AMADEO M-AX mini OEHM UND REHBEIN GMBH


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