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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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