K-number	K192014
Device name	SYPMHONY OCT System
Applicant	Medos International SARL
Product code	NKG
Device class	Class II
Decision date	Jan 24, 2020
Decision	Substantially Equivalent
Regulation	888.3075

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Source

View the full FDA submission: accessdata.fda.gov

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SYPMHONY OCT System

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SYPMHONY OCT System