K-number	K193376
Device name	Visalis V500, Visalis S500
Applicant	Carl Zeiss Meditec, AG
Product code	HQC
Device class	Class II
Decision date	Jun 15, 2020
Decision	Substantially Equivalent
Regulation	886.4670

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Source

View the full FDA submission: accessdata.fda.gov

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Visalis V500, Visalis S500

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