Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine

FDA 510(k) K213892 · Rb Health (Us), LLC

Substantially Equivalent

510(k) numberK213892

Submission

Device name
Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine
Applicant
Rb Health (Us), LLC
Parsippany, NJ, US
Received
December 14, 2021
Decision date
March 7, 2023
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 Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine cleared by the FDA?

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine (K213892) received a 510(k) decision of Substantially Equivalent on March 7, 2023, 448 days after the submission was received.

What is the product code of K213892?

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