K-number	K233676
Device name	Us2.v2
Applicant	Eko.Ai Pte Ltd. D/B/A Us2.Ai
Product code	QIH
Device class	Class II
Decision date	Apr 1, 2024
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Us2.v2

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