K-number	K012977
Device name	VARICES INJECTION NEEDLE
Applicant	Endo-Therapeutics, Inc.
Product code	FBK
Device class	Class II
Decision date	Nov 2, 2001
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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VARICES INJECTION NEEDLE

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