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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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