eUnity
K-Number: K161515 · 2016-11-15
Device Summary
Frequently Asked Questions
What is the eUnity?
eUnity is a medical device that received FDA 510(k) clearance on 2016-11-15. The listed applicant is Client Outlook, Inc.. The 510(k) number is K161515.
When did eUnity receive FDA 510(k) clearance?
eUnity received FDA 510(k) clearance on 2016-11-15, under 510(k) number K161515.
Who is the listed applicant for eUnity?
The FDA 510(k) record lists Client Outlook, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for eUnity?
The FDA product code for eUnity is LLZ.
Other records listing Client Outlook, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LLZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.