K-number	K012519
Device name	ARTHROCARE ELECTROSURGERY WANDS
Applicant	Arthrocare Corp.
Product code	GEI
Device class	Class II
Decision date	Oct 25, 2001
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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ARTHROCARE ELECTROSURGERY WANDS

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