K-Y Marilyn Pleasure Gel
K-Number: K151884 · 2016-01-11
ApplicantReckitt Benckiser, LLC
Decision Date2016-01-11
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
K-Y Marilyn Pleasure Gel is a medical device manufactured by Reckitt Benckiser, LLC. It received FDA 510(k) clearance on 2016-01-11 under approval number K151884. 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 K-Y Marilyn Pleasure Gel?
K-Y Marilyn Pleasure Gel is a medical device that received FDA 510(k) clearance on 2016-01-11. It is manufactured by Reckitt Benckiser, LLC. The 510(k) number is K151884.
When was K-Y Marilyn Pleasure Gel approved by the FDA?
K-Y Marilyn Pleasure Gel received FDA 510(k) clearance on 2016-01-11, under approval number K151884.
What company makes K-Y Marilyn Pleasure Gel?
K-Y Marilyn Pleasure Gel is manufactured by Reckitt Benckiser, LLC.
What is the FDA product code for K-Y Marilyn Pleasure Gel?
The FDA product code for K-Y Marilyn Pleasure Gel 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.