K-number	K234033
Device name	ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)
Applicant	Boehringer Laboratories, LLC
Product code	KNT
Device class	Class II
Decision date	May 6, 2024
Decision	Substantially Equivalent
Regulation	876.5980

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View the full FDA submission: accessdata.fda.gov

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ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)

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