Medical Device Manufacturer · US , Great Neck , NY

Viatronix, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2000

Official Website

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.

FDA 510(k) Regulatory Record - Viatronix, Inc.

8 devices

1-8 of 8

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