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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