Viatronix, Inc. is one of 21528 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viatronix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VIATRONIX V3D-CARDIAC, REVISION 1.0, VIATRONIX V3D COLON, REVISION 1.3, VIATRONIX V3D VASCULAR, REVISION 1.0
8
Total
8
Cleared
0
Denied
Viatronix, Inc. has 8 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 8 cleared submissions from 2000 to 2008. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Viatronix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Viatronix, Inc.
8 devices
Cleared
Dec 05, 2008
VIATRONIX V3D-CARDIAC, REVISION 1.0
Radiology
25d
Cleared
Apr 19, 2004
VIATRONIX V3D COLON, REVISION 1.3
Radiology
90d
Cleared
Nov 05, 2003
VIATRONIX V3D VASCULAR, REVISION 1.0
Radiology
15d
Cleared
Aug 22, 2003
VIATRONIX V3D EXPLORER, REVISION 1.2
Radiology
10d
Cleared
Sep 06, 2002
VIATRONIX V3D EXPLORER
Radiology
15d
Cleared
Mar 07, 2002
VIATRONIX V3D COLON
Radiology
6d
Cleared
Dec 07, 2001
VIATRONIC V3D CALCIUM SCORING
Radiology
78d
Cleared
Nov 17, 2000
VIATRONIX VISUALIZATION SYSTEM (VVS)
Radiology
72d