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FDA 510(k)

Coconut Infused Hybrid Personal Lubricant

K-Number: K180712 · 2018-06-06

ApplicantUnited Consortium
Decision Date2018-06-06
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Coconut Infused Hybrid Personal Lubricant is a medical device manufactured by United Consortium. It received FDA 510(k) clearance on 2018-06-06 under approval number K180712. 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 Coconut Infused Hybrid Personal Lubricant?

Coconut Infused Hybrid Personal Lubricant is a medical device that received FDA 510(k) clearance on 2018-06-06. It is manufactured by United Consortium. The 510(k) number is K180712.

When was Coconut Infused Hybrid Personal Lubricant approved by the FDA?

Coconut Infused Hybrid Personal Lubricant received FDA 510(k) clearance on 2018-06-06, under approval number K180712.

What company makes Coconut Infused Hybrid Personal Lubricant?

Coconut Infused Hybrid Personal Lubricant is manufactured by United Consortium.

What is the FDA product code for Coconut Infused Hybrid Personal Lubricant?

The FDA product code for Coconut Infused Hybrid 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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