Vidar Systems Corp. - FDA 510(k) Cleared Devices
Recent clearances: TELERADPRO EDGE, DIAGNOSTICPRO EDGE, TELERADPRO
13
Total
13
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vidar Systems Corp. Radiology ✕
13 devices
Cleared
Jun 07, 2013
TELERADPRO EDGE
Radiology
88d
Cleared
Apr 29, 2013
DIAGNOSTICPRO EDGE
Radiology
69d
Cleared
Oct 07, 2010
TELERADPRO
Radiology
38d
Cleared
Jan 07, 2010
VIDAR DENTAL FILM DIGITIZER
Radiology
29d
Cleared
May 30, 2007
VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS
Radiology
30d
Cleared
Mar 16, 2007
VIDAR VISION 2000
Radiology
17d
Cleared
Mar 04, 2003
VIDAR BONE TRACK SYSTEM SOFTWARE
Radiology
76d
Cleared
Oct 01, 2001
EXPRESSSUITE
Radiology
178d
Cleared
Jan 20, 2000
MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205
Radiology
87d
Cleared
Jan 18, 2000
DIAGNOSTIC PRO, MODEL 12772, VXR-16, MODEL 13020, VXR-16 DOSIMETRY PRO, MODEL...
Radiology
85d
Cleared
Dec 15, 1999
PLLL, TELERADPRO, MODEL 12714/12715, VXR-12 PLUS, MODEL 8619/9617
Radiology
51d
Cleared
Apr 17, 1998
VIDAR VXR LS LASER FILM DIGITIZER
Radiology
151d
Cleared
Dec 13, 1993
MEDSCAN 12
Radiology
139d