K-number	K223818
Device name	Model 9160 VitaloQUB
Applicant	Vitalograph Ireland, Ltd.
Product code	JEH
Device class	Class II
Decision date	May 25, 2023
Decision	Substantially Equivalent
Regulation	868.1760

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View the full FDA submission: accessdata.fda.gov

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Model 9160 VitaloQUB

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