FDA 510(k) Applications Submitted by VIDAR SYSTEMS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K974315 11/17/1997 VIDAR VXR LS LASER FILM DIGITIZER VIDAR SYSTEMS CORP.
K130406 02/19/2013 DIAGNOSTICPRO EDGE VIDAR SYSTEMS CORP.
K130636 03/11/2013 TELERADPRO EDGE; TELERADPRO EDGE HD-CCD VIDAR SYSTEMS CORP.
K102476 08/30/2010 TELERADPRO VIDAR SYSTEMS CORP.
K093809 12/09/2009 VIDAR DENTAL FILM DIGITIZER VIDAR SYSTEMS CORP.
K071193 04/30/2007 VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS VIDAR SYSTEMS CORP.
K024171 12/18/2002 VIDAR BONE TRACK SYSTEM SOFTWARE VIDAR SYSTEMS CORP.
K070563 02/27/2007 VIDAR VISION 2000 VIDAR SYSTEMS CORP.
K011049 04/06/2001 EXPRESSSUITE VIDAR SYSTEMS CORP.
K993597 10/25/1999 PLLL, TELERADPRO, MODEL 12714/12715, VXR-12 PLUS, MODEL 8619/9617 VIDAR SYSTEMS CORP.
K993598 10/25/1999 MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205 VIDAR SYSTEMS CORP.
K993599 10/25/1999 DIAGNOSTIC PRO, MODEL 12772, VXR-16, MODEL 13020, VXR-16 DOSIMETRY PRO, MODEL 13019 VIDAR SYSTEMS CORP.


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