K-number	K192037
Device name	Advisor VL Circular Mapping Catheter, Sensor Enabled
Applicant	ABBOTT MEDICAL
Product code	DRF
Device class	Class II
Decision date	Sep 17, 2019
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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Advisor VL Circular Mapping Catheter, Sensor Enabled

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