K-number	K132206
Device name	MELYS ATRIAL FIBRILLATION SCREENING MONITOR
Applicant	Advanced Fluidics, LLC
Product code	DXH
Device class	Class II
Decision date	Mar 19, 2014
Decision	Substantially Equivalent
Regulation	870.2920

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Source

View the full FDA submission: accessdata.fda.gov

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MELYS ATRIAL FIBRILLATION SCREENING MONITOR

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