FDA 510(k) Applications Submitted by CARRIE L BRANCART

FDA 510(k) Number Submission Date Device Name Applicant
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.


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