K-number	K993995
Device name	VEIN ENTRY INDICATOR DEVICE (VEID)
Applicant	Vascular Technologies , Ltd.
Product code	FMF
Device class	Class II
Decision date	Feb 14, 2000
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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VEIN ENTRY INDICATOR DEVICE (VEID)

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