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FDA 510(k)

GLISSANT Intimate Lubricant

K-Number: K183050 · 2019-07-08

ApplicantVjuvenate, LLC
Decision Date2019-07-08
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GLISSANT Intimate Lubricant is a medical device manufactured by Vjuvenate, LLC. It received FDA 510(k) clearance on 2019-07-08 under approval number K183050. 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 GLISSANT Intimate Lubricant?

GLISSANT Intimate Lubricant is a medical device that received FDA 510(k) clearance on 2019-07-08. It is manufactured by Vjuvenate, LLC. The 510(k) number is K183050.

When was GLISSANT Intimate Lubricant approved by the FDA?

GLISSANT Intimate Lubricant received FDA 510(k) clearance on 2019-07-08, under approval number K183050.

What company makes GLISSANT Intimate Lubricant?

GLISSANT Intimate Lubricant is manufactured by Vjuvenate, LLC.

What is the FDA product code for GLISSANT Intimate Lubricant?

The FDA product code for GLISSANT Intimate 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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