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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