K-number	K962321
Device name	ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970
Applicant	Arthrocare Corp.
Product code	HRX
Device class	Class II
Decision date	Jul 19, 1996
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970

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