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FDA 510(k)

JO Gelato Flavored Personal Lubricants

K-Number: K172447 · 2017-10-31

ApplicantUnited Consortium
Decision Date2017-10-31
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JO Gelato Flavored Personal Lubricants is a medical device manufactured by United Consortium. It received FDA 510(k) clearance on 2017-10-31 under approval number K172447. 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 Gelato Flavored Personal Lubricants?

JO Gelato Flavored Personal Lubricants is a medical device that received FDA 510(k) clearance on 2017-10-31. It is manufactured by United Consortium. The 510(k) number is K172447.

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

JO Gelato Flavored Personal Lubricants received FDA 510(k) clearance on 2017-10-31, under approval number K172447.

What company makes JO Gelato Flavored Personal Lubricants?

JO Gelato Flavored Personal Lubricants is manufactured by United Consortium.

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

The FDA product code for JO Gelato 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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