K-number	K110986
Device name	OPTOMED SMARTSCOPE M5 EY3 AND M5 ES1
Applicant	Optomed OY
Product code	HKI
Device class	Class II
Decision date	May 16, 2011
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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OPTOMED SMARTSCOPE M5 EY3 AND M5 ES1

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