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FDA 510(k) Applications Submitted by ULTRASPECT LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040370
02/13/2004
WBR-FHR, WBR-FWB
ULTRASPECT LTD.
K080784
03/20/2008
WBR XPRESS.CARDIAC, WBR XPRESS.BONE; WBR XACT.CARDIAC, WBR XACT.BONE
ULTRASPECT LTD.
K050815
03/31/2005
XACT.CARDIAC & XPRESS.CARDIAC
ULTRASPECT LTD.
K091073
04/14/2009
WBR XPRESS.CARDIAC AND XPRESS3.CARDIAC INCLUDING ATTENUATION AND SCATTERING CORRECTIONS
ULTRASPECT LTD.
K081201
04/28/2008
WBR XPRESS3.CARDIAC
ULTRASPECT LTD.
K103710
12/20/2010
WBR XPRESS PET
ULTRASPECT LTD.
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