K-number	K233226
Device name	FlexView Diagnostic (v1.1.20)
Applicant	Radical Imaging, LLC
Product code	LLZ
Device class	Class II
Decision date	Jan 17, 2024
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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FlexView Diagnostic (v1.1.20)

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