K-number	K173034
Device name	FibroScan® Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+)
Applicant	Echosens
Product code	IYO
Device class	Class II
Decision date	Nov 14, 2017
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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FibroScan® Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+)

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