K-number	K083778
Device name	XENIUM XPH, MODELS 110, 130, 150, 170, 190 AND 210
Applicant	Baxter Healthcare Corporation
Product code	KDI
Device class	Class II
Decision date	Feb 20, 2009
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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XENIUM XPH, MODELS 110, 130, 150, 170, 190 AND 210

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