Cleared Traditional

K213671 - Astroglide Sensual Strawberry Personal Lubricant
(FDA 510(k) Clearance)

K213671 · Biofilm, Inc. · Obstetrics & Gynecology
Mar 2022
Decision
101d
Days
Class 2
Risk

K213671 is an FDA 510(k) clearance for the Astroglide Sensual Strawberry Personal Lubricant, a Lubricant, Personal (Class II — Special Controls, product code NUC), submitted by Biofilm, Inc. (Vista, US). The FDA issued a Cleared decision on March 3, 2022, 101 days after receiving the submission on November 22, 2021. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.5300.

Submission Details

510(k) Number K213671 FDA.gov
FDA Decision Cleared SESE
Date Received November 22, 2021
Decision Date March 03, 2022
Days to Decision 101 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF

Device Classification

Product Code NUC — Lubricant, Personal
Device Class Class II — Special Controls
CFR Regulation 21 CFR 884.5300
Definition 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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