K-number	K211156
Device name	CONVIVO In Vivo Pathology Suite
Applicant	Carl Zeiss Meditec, AG
Product code	LLZ
Device class	Class II
Decision date	Dec 29, 2021
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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CONVIVO In Vivo Pathology Suite

Everything you need for a 510(k) submission. Nothing you don't.