K-number	K240013
Device name	EchoGo Heart Failure (2.0)
Applicant	Ultromics Limited
Product code	QUO
Device class	Class II
Decision date	Sep 23, 2024
Decision	Substantially Equivalent
Regulation	870.2200

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Source

View the full FDA submission: accessdata.fda.gov

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EchoGo Heart Failure (2.0)

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