K-number	K943171
Device name	CROSSFIRE(TM) (705-10650)
Applicant	Cardiogenes
Product code	GEX
Device class	Class II
Decision date	Sep 20, 1994
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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CROSSFIRE(TM) (705-10650)

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