K-number	K170874
Device name	Eko Model E5 System (EME5), Eko DUO
Applicant	Eko Devices, Inc.
Product code	DQD
Device class	Class II
Decision date	May 19, 2017
Decision	Substantially Equivalent
Regulation	870.1875

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View the full FDA submission: accessdata.fda.gov

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Eko Model E5 System (EME5), Eko DUO

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