K-number	K051627
Device name	VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT
Applicant	Valleylab
Product code	GEI
Device class	Class II
Decision date	Jul 22, 2005
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT

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