K-number	K013139
Device name	STELLARTECH COAGULATION SYSTEM
Applicant	Stellartech Research Corp.
Product code	GEI
Device class	Class II
Decision date	Dec 18, 2001
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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STELLARTECH COAGULATION SYSTEM

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