K-number	K012325
Device name	CARDIOVENTION CORX SYSTEM, MODEL FG 0001
Applicant	Cardiovention, Inc.
Product code	KFM
Device class	Class II
Decision date	Apr 9, 2002
Decision	Substantially Equivalent
Regulation	870.4360

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View the full FDA submission: accessdata.fda.gov

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CARDIOVENTION CORX SYSTEM, MODEL FG 0001

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