K-number	K081201
Device name	WBR XPRESS3.CARDIAC
Applicant	Ultraspect , Ltd.
Product code	KPS
Device class	Class II
Decision date	May 28, 2008
Decision	Substantially Equivalent
Regulation	892.1200

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View the full FDA submission: accessdata.fda.gov

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WBR XPRESS3.CARDIAC

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