Marathon No Sting Liquid Skin Protectant

FDA 510(k) K133443 · Advanced Medical Solutions (Plymouth), Ltd.

Substantially Equivalent

510(k) numberK133443

Submission

Device name
Marathon No Sting Liquid Skin Protectant
Applicant
Advanced Medical Solutions (Plymouth), Ltd.
Plympton, Plymouth, Devon, GB
Received
November 12, 2013
Decision date
July 10, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KMF – Bandage, Liquid
Device class
Class I (low risk)
Regulation
21 CFR 880.5090
Specialty
General Hospital

Other 510(k)s with product code KMF

510(k)DeviceApplicantDecision
K241916TearRepair Liquid Skin ProtectantKMF · Traditional Optmed, Inc.09/27/2024SE
K182733Rochal Bioshield Silicone FilmKMF · Traditional Rochal Industries, LLC06/27/2019SE
K171148Aleo BME Liquid BandageKMF · Traditional Aleo Bme, Inc.01/12/2018SE
K153571Cavilon Advanced High Endurance Skin ProtectantKMF · Traditional 3M Healthcare08/23/2016SE
K160684Atteris No-Sting Skin ProtectantKMF · Traditional Rochal Industries, LLC07/26/2016SE
K131384Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid BandageKMF · Traditional Kericure, Inc.08/07/2014SE
K120059Liquid BandageKMF · Traditional Chesson Laboratory Associates, Inc.05/17/2012SE
K092712Skin Barrier FilmKMF · Traditional Lodestar Products, Inc.02/23/2010SE
K083087EcocelKMF · Traditional Polichem S.A08/07/2009SE
K083913Chesson Labs Liquid BandageKMF · Traditional Chesson Laboratory Associates, Inc.07/31/2009SE

More from Chesson Laboratory Associates, Inc.

510(k)DeviceDecision
K151182LiquiBand ExceedMPN · Traditional 10/26/2015SE
K132243Barle Tissue Adhesive 2MPN · Traditional 12/20/2013SE
K123133Barle Tissue AdhesiveMPN · Traditional 05/22/2013SE
K122446Liquidband Flow ControlMPN · Traditional 10/26/2012SE

Questions and answers

When was Marathon No Sting Liquid Skin Protectant cleared by the FDA?

Marathon No Sting Liquid Skin Protectant (K133443) received a 510(k) decision of Substantially Equivalent on July 10, 2014, 240 days after the submission was received.

What is the product code of K133443?

The FDA product code is KMF – Bandage, Liquid, a Class I (low risk) device regulated under 21 CFR 880.5090.