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FDA 510(k)

JO Agapé Personal Lubricant

K-Number: K171021 · 2017-07-18

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

Device Summary

JO Agapé Personal Lubricant is a medical device manufactured by United Consortium. It received FDA 510(k) clearance on 2017-07-18 under approval 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. It is manufactured by United Consortium. The 510(k) number is K171021.

When was JO Agapé Personal Lubricant approved by the FDA?

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

What company makes JO Agapé Personal Lubricant?

JO Agapé Personal Lubricant is manufactured by United Consortium.

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

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

Other Devices by United Consortium

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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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