K-number	K180848
Device name	AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches
Applicant	ArthroCare Corporation
Product code	GEI
Device class	Class II
Decision date	May 1, 2018
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches

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