K-number	K160290
Device name	Valleylab REM Polyhesive Infant Patient Return Electrode
Applicant	Covidien, LLC
Product code	GEI
Device class	Class II
Decision date	May 19, 2016
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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Valleylab REM Polyhesive Infant Patient Return Electrode

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