K-number	K965066
Device name	ARRHYTHMIA MAPPING SYSTEM (8100/8300)
Applicant	Cardiac Pathways Corp.
Product code	DRF
Device class	Class II
Decision date	Aug 11, 1997
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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ARRHYTHMIA MAPPING SYSTEM (8100/8300)

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