K-number	K052297
Device name	POREX ELECTROSURGERY NEEDLE
Applicant	Porex Surgical, Inc.
Product code	GEI
Device class	Class II
Decision date	Mar 28, 2006
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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POREX ELECTROSURGERY NEEDLE

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