Cleared Traditional

Nitrile Examination Gloves (K210776) - FDA 510(k) Clearance

Class I General Hospital device.

K210776 · 5r Med Instruments (Chengdu) Co., Ltd. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2021
Decision
119d
Days
Class 1
Risk

K210776 is an FDA 510(k) clearance for the Nitrile Examination Gloves. Classified as Polymer Patient Examination Glove (product code LZA), Class I - General Controls.

Submitted by 5r Med Instruments (Chengdu) Co., Ltd. (Chengdu, CN). The FDA issued a Cleared decision on July 12, 2021 after a review of 119 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 5r Med Instruments (Chengdu) Co., Ltd. devices

Submission Details

510(k) Number K210776 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 2021
Decision Date July 12, 2021
Days to Decision 119 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
10d faster than avg
Panel avg: 129d · This submission: 119d
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 Consultant

Shanghai Truthful Information Technology Co., Ltd.
Boyle Wang

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

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 K210776.
Disposable Nitrile Medical Examination Glove
K210684 · Jiangsu Cureguard Glove Co., Ltd. · Jul 2021
Edma Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)
K211547 · Edma Group, LLC · Jul 2021
Nitrile Patient Examination Glove
K210723 · Jiangxi Zhonghong Pulin Medical Products Co., Ltd. · Jul 2021
Medical Nitrile Examination Gloves (Power free, Blue)
K210578 · Jiangxi Hongda Medical Equipment Group , Ltd. · Jul 2021
Violet Nitrile Powder Free Patient Examination Glove, Non Sterile
K210587 · Onetexx Sdn Bhd · Jun 2021
White Nitrile Powder Free Patient Examination Glove, Non Sterile
K210775 · Onetexx Sdn Bhd · Jun 2021