K-number	K963658
Device name	EXEL AVF SINGLE NEEDLE
Applicant	Exel Intl.
Product code	FMI
Device class	Class II
Decision date	May 5, 1998
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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EXEL AVF SINGLE NEEDLE

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