K-number	K925581
Device name	BAXTER BIOSTAT 1000 UREA MONITOR
Applicant	Baxter Healthcare Corp
Product code	KXM
Device class	Class II
Decision date	May 3, 1995
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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BAXTER BIOSTAT 1000 UREA MONITOR

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