K-number	K101991
Device name	WEBSTER DUO-DECAPOLAR CATHETER
Applicant	Biosense Webster, Inc.
Product code	DRF
Device class	Class II
Decision date	May 2, 2011
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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WEBSTER DUO-DECAPOLAR CATHETER

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