Astroglide Sensual Strawberry

FDA 510(k) K140590 · Biofilm, Inc.

Substantially Equivalent

510(k) numberK140590

Submission

Device name
Astroglide Sensual Strawberry
Applicant
Biofilm, Inc.
Vista, CA, US
Received
March 7, 2014
Decision date
October 30, 2014
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 Astroglide Sensual Strawberry cleared by the FDA?

Astroglide Sensual Strawberry (K140590) received a 510(k) decision of Substantially Equivalent on October 30, 2014, 237 days after the submission was received.

What is the product code of K140590?

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