FDA 510(k) Applications Submitted by VIATRONIX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K040126 01/20/2004 VIATRONIX V3D COLON, REVISION 1.3 VIATRONIX, INC.
K020658 03/01/2002 VIATRONIX V3D COLON VIATRONIX, INC.
K083293 11/10/2008 VIATRONIX V3D-CARDIAC, REVISION 1.0 VIATRONIX, INC.
K033361 10/21/2003 VIATRONIX V3D VASCULAR, REVISION 1.0 VIATRONIX, INC.
K022789 08/22/2002 VIATRONIX V3D EXPLORER VIATRONIX, INC.
K032483 08/12/2003 VIATRONIX V3D EXPLORER, REVISION 1.2 VIATRONIX, INC.
K002780 09/06/2000 VIATRONIX VISUALIZATION SYSTEM (VVS) VIATRONIX, INC.
K013146 09/20/2001 VIATRONIC V3D CALCIUM SCORING VIATRONIX, INC.


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