K-number	K162074
Device name	Werewolf RF20000 Controller, FLOW 50 Wand
Applicant	ArthroCare Corporation
Product code	GEI
Device class	Class II
Decision date	Aug 22, 2016
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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Werewolf RF20000 Controller, FLOW 50 Wand

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