K-number	K182013
Device name	EasyInstruments
Applicant	Agency For Medical Innovations GmbH
Product code	GEI
Device class	Class II
Decision date	Mar 11, 2019
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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EasyInstruments

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