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FDA 510(k)

JO Agapé Personal Lubricant

K-Number: K171021 · 2017-07-18

Decision Date2017-07-18
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JO Agapé Personal Lubricant is the device name listed in this FDA 510(k) record. The listed applicant is United Consortium. It received FDA 510(k) clearance on 2017-07-18 under 510(k) number K171021. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JO Agapé Personal Lubricant?

JO Agapé Personal Lubricant is a medical device that received FDA 510(k) clearance on 2017-07-18. The listed applicant is United Consortium. The 510(k) number is K171021.

When did JO Agapé Personal Lubricant receive FDA 510(k) clearance?

JO Agapé Personal Lubricant received FDA 510(k) clearance on 2017-07-18, under 510(k) number K171021.

Who is the listed applicant for JO Agapé Personal Lubricant?

The FDA 510(k) record lists United Consortium as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JO Agapé Personal Lubricant?

The FDA product code for JO Agapé Personal Lubricant is NUC.

Other records listing United Consortium 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.

View all 13 devices →

Related Devices (Code: NUC)

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

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