K-number	K102913
Device name	FORCETRIAD
Applicant	Covidien, Formerly Valleylab, A Division of Tyco H
Product code	GEI
Device class	Class II
Decision date	May 6, 2011
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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FORCETRIAD

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