Luvena Enhanced Personal Moisturizer, Luvena Enhanced Personal Lubricant

FDA 510(k) K150841 · Laclede, Inc.

Substantially Equivalent

510(k) numberK150841

Submission

Device name
Luvena Enhanced Personal Moisturizer, Luvena Enhanced Personal Lubricant
Applicant
Laclede, Inc.
Rancho Dominguez, CA, US
Received
March 30, 2015
Decision date
December 29, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NUC – Lubricant, Personal
Device class
Class II (moderate risk)
Regulation
21 CFR 884.5300
Specialty
Obstetrics/Gynecology

This device is a personal lubricant, for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity, and supplement the body's natural lubrication. This product may or may not be compatible with natural rubber latex, polyisoprene, and/or polyurethane condoms.

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Questions and answers

When was Luvena Enhanced Personal Moisturizer, Luvena Enhanced Personal Lubricant cleared by the FDA?

Luvena Enhanced Personal Moisturizer, Luvena Enhanced Personal Lubricant (K150841) received a 510(k) decision of Substantially Equivalent on December 29, 2015, 274 days after the submission was received.

What is the product code of K150841?

The FDA product code is NUC – Lubricant, Personal, a Class II (moderate risk) device regulated under 21 CFR 884.5300.