K-number	K132362
Device name	WECK EFX ENDO FASCIAL CLOSURE SYSTEM
Applicant	Teleflexmedical, Inc.
Product code	OCW
Device class	Class II
Decision date	Oct 8, 2013
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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WECK EFX ENDO FASCIAL CLOSURE SYSTEM

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