K-number	K130717
Device name	ENDO GIA RELOAD
Applicant	Covidien, Formerly US Surgical A Divison of Tyco H
Product code	GDW
Device class	Class II
Decision date	Apr 18, 2013
Decision	Substantially Equivalent
Regulation	878.4750

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View the full FDA submission: accessdata.fda.gov

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ENDO GIA RELOAD

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