K-number	K241925
Device name	VitruvianScan (v1.0)
Applicant	Perspectum, Ltd.
Product code	LNH
Device class	Class II
Decision date	Oct 2, 2024
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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VitruvianScan (v1.0)

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