K-number	K900125
Device name	ARTERIOVENOUS FISTULA SETS
Applicant	Baxter Healthcare Corp
Product code	FIE
Device class	Class II
Decision date	Jan 31, 1990
Decision	Substantially Equivalent
Regulation	876.5540

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Source

View the full FDA submission: accessdata.fda.gov

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ARTERIOVENOUS FISTULA SETS

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