Cleared Traditional

K962069 - MEDLINE PRE-POWDERED NON-STERILE/STERILE VINYL EXAMINATION GLOVES

K962069 is an FDA 510(k) clearance for MEDLINE PRE-POWDERED NON-STERILE/STERIL..., manufactured by Medline Industries, Inc.. The device is a Class 1 General Hospital device with product code LYZ cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K962069 · Medline Industries, Inc. · General Hospital
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Aug 1996
Decision
83d
Days
Class 1
Risk

K962069 is an FDA 510(k) clearance for the MEDLINE PRE-POWDERED NON-STERILE/STERILE VINYL EXAMINATION GLOVES. Classified as Vinyl Patient Examination Glove (product code LYZ), Class I - General Controls.

Submitted by Medline Industries, Inc. (Mundelein, US). The FDA issued a Cleared decision on August 19, 1996 after a review of 83 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 Medline Industries, Inc. devices

FDA 510(k) Submission Details - K962069

510(k) Number K962069 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 28, 1996
Decision Date August 19, 1996
Days to Decision 83 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
46d faster than avg
Panel avg: 129d · This submission: 83d
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 372
Devices cleared under the same product code (LYZ) and FDA review panel - the closest regulatory comparables to K962069.
PACER PLUS SYNTHETIC MEDICAL VINLY PATIENT EXAMINATION GLOVES (POWDERED)
K963514 · Shanghai PM Plastics Enterise Co., Ltd. · Oct 1996
PACER PLUS SYNTHETIC MEDICAL VINYL PATIENT EXAMINATION GLOVE POWDER FREE
K963710 · Canopus Medical Supply Co., Ltd. · Oct 1996
PREPOWDER VINYL PATIENT EXAMINATION GLOVES
K962026 · Hong Huang Tang Industrial Co., Ltd. · Sep 1996
GLOVE, EXAMINATION, VINYL
K952050 · Oak Carolina, Inc. · Aug 1996
SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVES
K960746 · Sunmax Enterprise Shanghai Co. , Ltd. · Jun 1996
ARISTA VINYL EXAMINATION GLOVES
K954153 · Arista Latindo Industrial Ltd. P.T · Jan 1996