Latex Examination Gloves Non-Sterile

FDA 510(k) K890356 · Quest Intl., Inc.

Substantially Equivalent

510(k) numberK890356

Submission

Device name
Latex Examination Gloves Non-Sterile
Applicant
Quest Intl., Inc.
Fort Smith, AR, US
Received
January 24, 1989
Decision date
April 6, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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.

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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
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K221648Iconic Latex GloveLYY · Traditional Iconic Medicare Sdn Bhd08/25/2022SE

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Questions and answers

When was Latex Examination Gloves Non-Sterile cleared by the FDA?

Latex Examination Gloves Non-Sterile (K890356) received a 510(k) decision of Substantially Equivalent on April 6, 1989, 72 days after the submission was received.

What is the product code of K890356?

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