K-number	K173771
Device name	IOLMaster 700
Applicant	Carl Zeiss Meditec, AG
Product code	HJO
Device class	Class II
Decision date	Aug 24, 2018
Decision	Substantially Equivalent
Regulation	886.1850

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Source

View the full FDA submission: accessdata.fda.gov

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IOLMaster 700

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