Cleared Traditional

K110314 - STRETCH VINYL EXAMINATION GLOVE, POWDER FREE (YELLOW/WHITE/CLEAR(NON-COLORED)

K110314 is an FDA 510(k) clearance for STRETCH VINYL EXAMINATION GLOVE, manufactured by True Glove Factory. The device is a Class 1 General Hospital device with product code LYZ cleared through the Traditional 510(k) pathway after a 97-day FDA review.

K110314 · True Glove Factory · General Hospital
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May 2011
Decision
97d
Days
Class 1
Risk

K110314 is an FDA 510(k) clearance for the STRETCH VINYL EXAMINATION GLOVE, POWDER FREE (YELLOW/WHITE/CLEAR(NON-COLORED). Classified as Vinyl Patient Examination Glove (product code LYZ), Class I - General Controls.

Submitted by True Glove Factory (Weifang, Shandong, CN). The FDA issued a Cleared decision on May 10, 2011 after a review of 97 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.

FDA 510(k) Submission Details - K110314

510(k) Number K110314 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 02, 2011
Decision Date May 10, 2011
Days to Decision 97 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
32d faster than avg
Panel avg: 129d · This submission: 97d
Pathway characteristics
Predicate-based equivalence.

LYZ Device Classification - Class 1, General Controls

Product Code LYZ Vinyl Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Vinyl Patient Examination Glove Is A Disposable Device Made Of Poly(vinyl Chloride) 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 - LYZ Vinyl Patient Examination Glove

All 749
Devices cleared under the same product code (LYZ) and FDA review panel - the closest regulatory comparables to K110314.
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, LIGHT YELLOW COLOR
K111459 · Jiangsu Alfa Glove Co., Ltd. · Jun 2011
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
K110969 · Ppp Medical and Safety Products Company Limited · Jun 2011
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, LIGHT YELLOW COLOR
K110972 · Ppp Medical and Safety Products Company Limited · Jun 2011
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K103196 · Changda Plastic Product Co., Ltd. · Apr 2011
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K102152 · Hebei Tengda Plastic Co., Ltd. · Apr 2011
POWDERED VINYL PATIENT EXAMINATION GLOVES
K102151 · Hebei Tengda Plastic Co., Ltd. · Apr 2011
K110314 · STRETCH VINYL EXAMINATION GLOVE, POWDER FREE (YELLOW/WHITE/CLEAR(NON-COLORED)
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