Home / Companies / Vidar Systems Corp.

Vidar Systems Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDJune 7, 2013
K130406DIAGNOSTICPRO EDGEApril 29, 2013
K102476TELERADPROOctober 7, 2010
K093809VIDAR DENTAL FILM DIGITIZERJanuary 7, 2010
K071193VIDAR VISION 3000 AND 4000 X-RAY SYSTEMSMay 30, 2007
K070563VIDAR VISION 2000March 16, 2007
K024171VIDAR BONE TRACK SYSTEM SOFTWAREMarch 4, 2003
K011049EXPRESSSUITEOctober 1, 2001
K993598MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205January 20, 2000
K993599DIAGNOSTIC PRO, MODEL 12772, VXR-16, MODEL 13020, VXR-16 DOSIMETRY PRO, MODEL 13019January 18, 2000
K993597PLLL, TELERADPRO, MODEL 12714/12715, VXR-12 PLUS, MODEL 8619/9617December 15, 1999
K974315VIDAR VXR LS LASER FILM DIGITIZERApril 17, 1998
K933632MEDSCAN 12December 13, 1993