Cleared Traditional

K020751 - SYNTEX POWDER-FREE POLYMER-COATED NITRILE EXAMINATION GLOVE

K020751 is an FDA 510(k) clearance for SYNTEX POWDER-FREE POLYMER-COATED NITRI..., manufactured by Syntex Healthcare Products Co., Ltd.. The device is a Class 1 General Hospital device with product code LZA cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K020751 · Syntex Healthcare Products Co., Ltd. · General Hospital
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May 2002
Decision
56d
Days
Class 1
Risk

K020751 is an FDA 510(k) clearance for the SYNTEX POWDER-FREE POLYMER-COATED NITRILE EXAMINATION GLOVE. Classified as Polymer Patient Examination Glove (product code LZA), Class I - General Controls.

Submitted by Syntex Healthcare Products Co., Ltd. (Xinji City, Hebei Province, CN). The FDA issued a Cleared decision on May 2, 2002 after a review of 56 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Syntex Healthcare Products Co., Ltd. devices

FDA 510(k) Submission Details - K020751

510(k) Number K020751 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 2002
Decision Date May 02, 2002
Days to Decision 56 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 129d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

LZA Device Classification - Class 1, General Controls

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 1157
Devices cleared under the same product code (LZA) and FDA review panel - the closest regulatory comparables to K020751.
SHANGHAI GLOVMAX ENTERPRISE POWDERFREE BLUE NITRILE EXAMINATION GLOVES
K021001 · Shanghai Glovmax Enterprise Co.,Ltd · May 2002
DERMAGRIP AND MULTIPLE POWDER FREE PURPLE NITRILE EXAMINATION GLOVES, NON-STERILE
K021396 · Wrp Specialty Products Sdn. Bhd. · May 2002
GLOVCO POWDER-FREE NITRILE EXAMINATION GLOVES
K021308 · Glovco (M) Sdn. Bhd. · May 2002
CASHMERE NON-STERILE, POWDER FREE NITRILE EXAMINATION GLOVES (WHITE)
K020868 · Seal Polymer Industries Bhd. · Apr 2002
CHLORINATED POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH ALOE VERA
K013774 · Supermax Sdn Bhd · Mar 2002
SYNTEX POWDER-FREE NITRILE EXAMINATION GLOVE
K020493 · Syntex Healthcare Products Co., Ltd. · Feb 2002