K-number	K002021
Device name	HEMOSTATIX THERMAL SCALPEL SYSTEM - #12 BLADE
Applicant	Gyrus Ent LLC
Product code	GEI
Device class	Class II
Decision date	Aug 24, 2000
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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HEMOSTATIX THERMAL SCALPEL SYSTEM - #12 BLADE

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