K-number	K052857
Device name	ELECTROSURGICAL GENERATOR SYSTEM, MODEL ES 3000
Applicant	Senorx, Inc.
Product code	GEI
Device class	Class II
Decision date	Oct 21, 2005
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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ELECTROSURGICAL GENERATOR SYSTEM, MODEL ES 3000

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