Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Ultraspect , Ltd.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K103710	WBR XPRESS PET	KPS	2011-01-19	View
510(k)	K091073	WBR XPRESS.CARDIAC AND XPRESS3.CARDIAC INCLUDING ATTENUATION AND SCATTERING CORRECTIONS	KPS	2009-05-14	View
510(k)	K081201	WBR XPRESS3.CARDIAC	KPS	2008-05-28	View
510(k)	K080784	WBR XPRESS.CARDIAC, WBR XPRESS.BONE; WBR XACT.CARDIAC, WBR XACT.BONE	KPS	2008-04-02	View
510(k)	K050815	XACT.CARDIAC & XPRESS.CARDIAC	KPS	2005-04-26	View
510(k)	K040370	WBR-FHR, WBR-FWB	KPS	2004-03-11	View

↑