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FDA 510(k)

EasyInstruments

K-Number: K182013 · 2019-03-11

ApplicantAgency For Medical Innovations GmbH
Decision Date2019-03-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EasyInstruments is a medical device manufactured by Agency For Medical Innovations GmbH. It received FDA 510(k) clearance on 2019-03-11 under approval number K182013. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EasyInstruments?

EasyInstruments is a medical device that received FDA 510(k) clearance on 2019-03-11. It is manufactured by Agency For Medical Innovations GmbH. The 510(k) number is K182013.

When was EasyInstruments approved by the FDA?

EasyInstruments received FDA 510(k) clearance on 2019-03-11, under approval number K182013.

What company makes EasyInstruments?

EasyInstruments is manufactured by Agency For Medical Innovations GmbH.

What is the FDA product code for EasyInstruments?

The FDA product code for EasyInstruments is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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