K-number	K211219
Device name	LASSOSTAR NAV Circular Mapping Catheter
Applicant	Biosense Webster, Inc.
Product code	DRF
Device class	Class II
Decision date	Jan 26, 2022
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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LASSOSTAR NAV Circular Mapping Catheter

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