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FDA 510(k)

eego amplifiers

K-Number: K172312 · 2018-03-30

Decision Date2018-03-30
Product CodeGWL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

eego amplifiers is a medical device manufactured by Eemagine Medical Imaging Solutions GmbH. It received FDA 510(k) clearance on 2018-03-30 under approval number K172312. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the eego amplifiers?

eego amplifiers is a medical device that received FDA 510(k) clearance on 2018-03-30. It is manufactured by Eemagine Medical Imaging Solutions GmbH. The 510(k) number is K172312.

When was eego amplifiers approved by the FDA?

eego amplifiers received FDA 510(k) clearance on 2018-03-30, under approval number K172312.

What company makes eego amplifiers?

eego amplifiers is manufactured by Eemagine Medical Imaging Solutions GmbH.

What is the FDA product code for eego amplifiers?

The FDA product code for eego amplifiers is GWL.

Other Devices by Eemagine Medical Imaging Solutions GmbH

Related Devices (Code: GWL)

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.