K-number	K170170
Device name	Valleylab FT10 Electrosurgical Platform
Applicant	Covidien, LLC
Product code	GEI
Device class	Class II
Decision date	Feb 16, 2017
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Valleylab FT10 Electrosurgical Platform

Everything you need for a 510(k) submission. Nothing you don't.