Cleared Traditional

Disposable Medical Nitrile Examination Gloves (Non sterile) (QN-N001, QN-N002, QN-N003, QN-N004, QN-N005) (K240824) - FDA 510(k) Clearance

Class I General Hospital device.

K240824 · Ningxia Qiaoen Medical Technology Co., Ltd. · General Hospital
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Jun 2024
Decision
91d
Days
Class 1
Risk

K240824 is an FDA 510(k) clearance for the Disposable Medical Nitrile Examination Gloves (Non sterile) (QN-N001, QN-N002.... Classified as Polymer Patient Examination Glove (product code LZA), Class I - General Controls.

Submitted by Ningxia Qiaoen Medical Technology Co., Ltd. (Yinchuan, CN). The FDA issued a Cleared decision on June 25, 2024 after a review of 91 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6250 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Ningxia Qiaoen Medical Technology Co., Ltd. devices

Submission Details

510(k) Number K240824 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 2024
Decision Date June 25, 2024
Days to Decision 91 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
38d faster than avg
Panel avg: 129d · This submission: 91d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LZA Polymer Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
Definition 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.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - LZA Polymer Patient Examination Glove

All 489
Devices cleared under the same product code (LZA) and FDA review panel - the closest regulatory comparables to K240824.
Nitrile Powder Free Examination Gloves (Blue), Non-Sterile Low Dermatitis Potential
K241528 · Comfort Rubber Gloves Industries Sdn. Bhd. · Aug 2024
Powder Free Nitrile Examination Gloves (Blue), Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (XS,S,M,L,XL,XXL)
K241970 · Kanglongda Vietnam Protection Technology Company Limited · Aug 2024
Non-sterile, Powder-Free Nitrile Examination Glove Tested for use with 55 Chemotherapy Drugs and Fentanyl- Violet Blue
K240930 · Sri Trang Gloves (Thailand) Public Company Limited · Jul 2024
Nitrile Disposable Examination Gloves, Tested for Use with Chemotherapy Drugs and Fentanyl
K240629 · Xingyu Medical Tech Co., Ltd. · May 2024
Non-sterile, Powder-Free Nitrile Examination Glove Tested for use with Chemotherapy Drugs and Fentanyl (White, Black, and Violet Blue)
K232614 · Sri Trang Gloves (Thailand) Public Company Limited · May 2024
Black Pearl Nitrile Examination Glove
K232319 · Ug Global Resources Sdn. Bhd. · Apr 2024