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FDA 510(k)

eUnity

K-Number: K172490 · 2018-02-06

ApplicantClient Outlook, Inc.
Decision Date2018-02-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

eUnity is a medical device manufactured by Client Outlook, Inc.. It received FDA 510(k) clearance on 2018-02-06 under approval number K172490. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the eUnity?

eUnity is a medical device that received FDA 510(k) clearance on 2018-02-06. It is manufactured by Client Outlook, Inc.. The 510(k) number is K172490.

When was eUnity approved by the FDA?

eUnity received FDA 510(k) clearance on 2018-02-06, under approval number K172490.

What company makes eUnity?

eUnity is manufactured by Client Outlook, Inc..

What is the FDA product code for eUnity?

The FDA product code for eUnity is LLZ.

Other Devices by Client Outlook, Inc.

K161515eUnity

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Official Source

View on FDA Database →

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

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