K-number	K223426
Device name	ECHELON Synergy MRI system
Applicant	Fujifilm Healthcare Corporation
Product code	LNH
Device class	Class II
Decision date	Jul 13, 2023
Decision	Substantially Equivalent
Regulation	892.1000

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Source

View the full FDA submission: accessdata.fda.gov

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ECHELON Synergy MRI system

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