K-number	K212008
Device name	Reveal LINQ Insertable Cardiac Monitor
Applicant	Medtronic, Inc.
Product code	MXD
Device class	Class II
Decision date	Jul 22, 2021
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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Reveal LINQ Insertable Cardiac Monitor

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