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FDA 510(k)

Personal Lubricating Jelly

K-Number: K180923 · 2018-07-09

ApplicantPerrigo New York, Inc.
Decision Date2018-07-09
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Personal Lubricating Jelly is a medical device manufactured by Perrigo New York, Inc.. It received FDA 510(k) clearance on 2018-07-09 under approval number K180923. 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 Personal Lubricating Jelly?

Personal Lubricating Jelly is a medical device that received FDA 510(k) clearance on 2018-07-09. It is manufactured by Perrigo New York, Inc.. The 510(k) number is K180923.

When was Personal Lubricating Jelly approved by the FDA?

Personal Lubricating Jelly received FDA 510(k) clearance on 2018-07-09, under approval number K180923.

What company makes Personal Lubricating Jelly?

Personal Lubricating Jelly is manufactured by Perrigo New York, Inc..

What is the FDA product code for Personal Lubricating Jelly?

The FDA product code for Personal Lubricating Jelly 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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