Personal Lubricating Jelly
K-Number: K180923 · 2018-07-09
Device Summary
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. The listed applicant is Perrigo New York, Inc.. The 510(k) number is K180923.
When did Personal Lubricating Jelly receive FDA 510(k) clearance?
Personal Lubricating Jelly received FDA 510(k) clearance on 2018-07-09, under 510(k) number K180923.
Who is the listed applicant for Personal Lubricating Jelly?
The FDA 510(k) record lists Perrigo New York, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Personal Lubricating Jelly?
The FDA product code for Personal Lubricating Jelly is NUC.
Related Devices (Code: NUC)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.