K-number	K082319
Device name	INJEKT FILIFORM INJECTION NEEDLE
Applicant	Cook Urological, Inc.
Product code	FBK
Device class	Class II
Decision date	Sep 25, 2008
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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INJEKT FILIFORM INJECTION NEEDLE

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