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FDA 510(k)

JO Classic Hybrid Personal Lubricant

K-Number: K181408 · 2018-08-27

Decision Date2018-08-27
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JO Classic Hybrid Personal Lubricant is a medical device manufactured by United Consortium. It received FDA 510(k) clearance on 2018-08-27 under approval number K181408. 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 Classic Hybrid Personal Lubricant?

JO Classic Hybrid Personal Lubricant is a medical device that received FDA 510(k) clearance on 2018-08-27. It is manufactured by United Consortium. The 510(k) number is K181408.

When was JO Classic Hybrid Personal Lubricant approved by the FDA?

JO Classic Hybrid Personal Lubricant received FDA 510(k) clearance on 2018-08-27, under approval number K181408.

What company makes JO Classic Hybrid Personal Lubricant?

JO Classic Hybrid Personal Lubricant is manufactured by United Consortium.

What is the FDA product code for JO Classic Hybrid Personal Lubricant?

The FDA product code for JO Classic Hybrid Personal Lubricant is NUC.

Other Devices by United Consortium

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Related Devices (Code: NUC)

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.