K-number	K150251
Device name	Barrx Anorectal RFA Wand
Applicant	Covidien, LLC
Product code	GEI
Device class	Class II
Decision date	Jul 28, 2015
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Barrx Anorectal RFA Wand

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