K-number	K211328
Device name	EIDON FA, EIDON, EIDON AF, EIDON UWFL
Applicant	Centervue S.P.A.
Product code	MYC
Device class	Class II
Decision date	Aug 19, 2021
Decision	Substantially Equivalent
Regulation	886.1570

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View the full FDA submission: accessdata.fda.gov

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EIDON FA, EIDON, EIDON AF, EIDON UWFL

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