Cleared Traditional

K171985 - Astroglide O Oil Personal Lubricant & Massage Oil
(FDA 510(k) Clearance)

Aug 2017
Decision
58d
Days
Class 2
Risk

K171985 is an FDA 510(k) clearance for the Astroglide O Oil Personal Lubricant & Massage Oil. This device is classified as a Lubricant, Personal (Class II - Special Controls, product code NUC).

Submitted by Biofilm, Inc. (Vista, US). The FDA issued a Cleared decision on August 30, 2017, 58 days after receiving the submission on July 3, 2017.

This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5300. 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..

Submission Details

510(k) Number K171985 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 03, 2017
Decision Date August 30, 2017
Days to Decision 58 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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