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FDA 510(k)

JO H2O Flavored Personal Lubricants

K-Number: K180219 · 2018-04-20

ApplicantUnited Consortium
Decision Date2018-04-20
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JO H2O Flavored Personal Lubricants is a medical device manufactured by United Consortium. It received FDA 510(k) clearance on 2018-04-20 under approval number K180219. 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 H2O Flavored Personal Lubricants?

JO H2O Flavored Personal Lubricants is a medical device that received FDA 510(k) clearance on 2018-04-20. It is manufactured by United Consortium. The 510(k) number is K180219.

When was JO H2O Flavored Personal Lubricants approved by the FDA?

JO H2O Flavored Personal Lubricants received FDA 510(k) clearance on 2018-04-20, under approval number K180219.

What company makes JO H2O Flavored Personal Lubricants?

JO H2O Flavored Personal Lubricants is manufactured by United Consortium.

What is the FDA product code for JO H2O Flavored Personal Lubricants?

The FDA product code for JO H2O Flavored Personal Lubricants 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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