Powder Free Natural Rubber Latex Examination Gloves – Blue, Non-Sterile and Protein Claim Of 50 Micrograms per dm2 Or Less Protein

FDA 510(k) K250069 · Comfort Rubber Gloves Industries Sdn. Bhd.

Substantially Equivalent

510(k) numberK250069

Submission

Device name
Powder Free Natural Rubber Latex Examination Gloves – Blue, Non-Sterile and Protein Claim Of 50 Micrograms per dm2 Or Less Protein
Applicant
Comfort Rubber Gloves Industries Sdn. Bhd.
Matang, MY
Received
January 10, 2025
Decision date
April 29, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LYY – Latex Patient Examination Glove
Device class
Class I (low risk)
Regulation
21 CFR 880.6250
Specialty
General Hospital

A latex patient examination glove is a disposable device made of natural rubber latex that may or may not bear a trace amount of residual powder, and is intended to be worn on the hand for medical purposes to provide a barrier against potentially infectious materials and other contaminants.

Other 510(k)s with product code LYY

510(k)DeviceApplicantDecision
K240266Latex Examination Glove Powder Free (Ocean Blue and Natural White)LYY · Abbreviated Sri Trang Gloves (Thailand) Public Company Limited09/09/2024SE
K230573Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein…LYY · Traditional Kossan International Sdn Bhd06/13/2023SE
K223298Sterile Latex Examination Gloves Powder Free (S, M, L, Extra L)LYY · Traditional Shandong Intco Medical Products Co, Ltd.02/22/2023SE
K222612Powder-Free Latex examination glovesLYY · Traditional Guangdong Kingfa Sci. & Tech.Co., Ltd.11/25/2022SE
K221667Non Sterile Powder Free Latex Examination GloveLYY · Traditional New Era Medicare Sdn. Bhd.10/28/2022SE
K222348JR MedicLYY · Abbreviated Jr Engineering & Medical Technologies (M) Sdn.…10/27/2022SE
K221374Disposable Medical Rubber Examination Gloves (XS/S/M/L/XL)LYY · Traditional Hebei Titans Hongsen Medical Technology Co., Ltd.10/26/2022SE
K222693Single-use medical latex examination gloves (LG100)LYY · Traditional Fitone Latex Products Co., Ltd. Guangdong09/24/2022SE
K221648Iconic Latex GloveLYY · Traditional Iconic Medicare Sdn Bhd08/25/2022SE
K211601Powder Free Latex Examination Glove, Non-SterileLYY · Traditional Wrp Asia Pacific Sdn. Bhd.08/22/2022SE

More from Wrp Asia Pacific Sdn. Bhd.

510(k)DeviceDecision
K240269Nitrile Powder Free Examination Gloves Biodegradable (Green)LZA · Traditional 10/25/2024SE
K241528Nitrile Powder Free Examination Gloves (Blue), Non-Sterile Low Dermatitis PotentialLZA · Traditional 08/06/2024SE
K192954Power Free Nitrile Examination Gloves Tested for Use with Chemotherapy Drugs and FentanylLZA · Traditional 06/19/2020SE
K200181Black Colored Powder Free Nitrile Examination Gloves Tested for Use with Chemotherapy…LZA · Traditional 04/15/2020SE
K190080Powder Free Nitrile Examination Gloves Tested for Use with Chemotherapy Drugs Labeling…LZA · Traditional 06/27/2019SE
K180476Powder Free Nitrile Examination Gloves Tested for Use with Chemotherapy DrugsLZC · Traditional 05/15/2018SE
K171541Powder Free Nitrile Examination Gloves (Orange)LZA · Traditional 09/20/2017SE
K162405Powder Free Nitrile Examination Gloves Tested For Use With Chemotherapy Drugs Labeling…LZA · Traditional 03/28/2017SE
K110297Powder Free Nitrile (Black) Examination GlovesLZA · Traditional 06/15/2011SE
K101917Comfort Rubber Gloves Ind.Sdn.Bhd.LYY · Traditional 10/29/2010SE

Questions and answers

When was Powder Free Natural Rubber Latex Examination Gloves – Blue, Non-Sterile and Protein Claim Of 50 Micrograms per dm2 Or Less Protein cleared by the FDA?

Powder Free Natural Rubber Latex Examination Gloves – Blue, Non-Sterile and Protein Claim Of 50 Micrograms per dm2 Or Less Protein (K250069) received a 510(k) decision of Substantially Equivalent on April 29, 2025, 109 days after the submission was received.

What is the product code of K250069?

The FDA product code is LYY – Latex Patient Examination Glove, a Class I (low risk) device regulated under 21 CFR 880.6250.