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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