K-number	K233687
Device name	ECHELON Synergy V10.0
Applicant	FUJIFILM Healthcare Americas Corporation
Product code	LNH
Device class	Class II
Decision date	May 3, 2024
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 V10.0

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