K-number	K021615
Device name	BAXTER ACCURA SYSTEM, MODEL 5M5660
Applicant	Baxter Healthcare Corp
Product code	KDI
Device class	Class II
Decision date	Nov 18, 2002
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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BAXTER ACCURA SYSTEM, MODEL 5M5660

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