K-number	K190132
Device name	Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter
Applicant	Medtronic
Product code	DRF
Device class	Class II
Decision date	Jul 30, 2019
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter

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