K-number	K232331
Device name	InVision Precision LVEF (LVEF)
Applicant	InVision Medical Technology Corporation
Product code	QIH
Device class	Class II
Decision date	Apr 25, 2024
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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InVision Precision LVEF (LVEF)

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