K-number	K842622
Device name	HEMO STATIC/ESU SCALPEL SYSTEM
Applicant	Oximetrix, Inc.
Product code	GEI
Device class	Class II
Decision date	Oct 23, 1984
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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HEMO STATIC/ESU SCALPEL SYSTEM

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