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FDA 510(k)

JO for Him H2O Gel Original Personal Lubricant

K-Number: K192203 · 2020-02-10

ApplicantUnited Consortium
Decision Date2020-02-10
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JO for Him H2O Gel Original Personal Lubricant is a medical device manufactured by United Consortium. It received FDA 510(k) clearance on 2020-02-10 under approval number K192203. 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 for Him H2O Gel Original Personal Lubricant?

JO for Him H2O Gel Original Personal Lubricant is a medical device that received FDA 510(k) clearance on 2020-02-10. It is manufactured by United Consortium. The 510(k) number is K192203.

When was JO for Him H2O Gel Original Personal Lubricant approved by the FDA?

JO for Him H2O Gel Original Personal Lubricant received FDA 510(k) clearance on 2020-02-10, under approval number K192203.

What company makes JO for Him H2O Gel Original Personal Lubricant?

JO for Him H2O Gel Original Personal Lubricant is manufactured by United Consortium.

What is the FDA product code for JO for Him H2O Gel Original Personal Lubricant?

The FDA product code for JO for Him H2O Gel Original Personal Lubricant is NUC.

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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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