Sasmar Original, Sasmar Classic

FDA 510(k) K131084 · Sasmar, Inc.

Substantially Equivalent

510(k) numberK131084

Submission

Device name
Sasmar Original, Sasmar Classic
Applicant
Sasmar, Inc.
Chicago, IL, US
Received
April 18, 2013
Decision date
September 13, 2013
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 Sasmar Original, Sasmar Classic cleared by the FDA?

Sasmar Original, Sasmar Classic (K131084) received a 510(k) decision of Substantially Equivalent on September 13, 2013, 148 days after the submission was received.

What is the product code of K131084?

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