K-number	K171672
Device name	065 Zenith, 074 Zenith
Applicant	Inneuroco, Inc.
Product code	DQY
Device class	Class II
Decision date	Oct 19, 2017
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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065 Zenith, 074 Zenith

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