Powder-Free Blue Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)

FDA 510(k) K051378 · Medline

Substantially Equivalent

510(k) numberK051378

Submission

Device name
Powder-Free Blue Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)
Applicant
Medline
Mundelein, IL, US
Received
May 26, 2005
Decision date
August 3, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

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

A nitrile (or polymer) patient examination glove is a disposable device made of nitrile rubber or synthetic polymers 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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K260794NON-STERILE POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WITH LICORICE ROOT EXTRACT…LZA · Traditional Kossan International Sdn Bhd08/18/2026SE
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K254285Nitrile Powder Free Examination Gloves Tested for Use with Chemotherapy Drugs – Aqua…LZA · Special Hartalega NGC Sdn. Bhd.07/20/2026SE
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K253824Powder Free Nitrile Examination Gloves Non-Sterile BlackLZA · Traditional Kanglongda Vietnam Protection Technology Company…06/18/2026SE
K260867Nitrile Powder Free Examination Gloves Tested for Use with Chemotherapy Drugs and…LZA · Special Hartalega NGC Sdn. Bhd.06/17/2026SE
K260806Nitrile Disposable Examination GlovesLZA · Traditional Vista Industries,, LLC06/03/2026SE

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Questions and answers

When was Powder-Free Blue Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) cleared by the FDA?

Powder-Free Blue Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) (K051378) received a 510(k) decision of Substantially Equivalent on August 3, 2005, 69 days after the submission was received.

What is the product code of K051378?

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