K-number	K172743
Device name	Natus VikingQuest
Applicant	Natus Neurology Incorporated
Product code	IKN
Device class	Class II
Decision date	Dec 19, 2017
Decision	Substantially Equivalent
Regulation	890.1375

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Source

View the full FDA submission: accessdata.fda.gov

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Natus VikingQuest

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