K-number	K023664
Device name	SYNTRA + DIALYZER, MODEL 200
Applicant	Baxter Healthcare Corp
Product code	KDI
Device class	Class II
Decision date	Feb 21, 2003
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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SYNTRA + DIALYZER, MODEL 200

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