Cleared Traditional

K935852 - COMFIT POWDER FREE EXAMINATION GLOVES (HYPOALLERGENIC)

K935852 is an FDA 510(k) clearance for COMFIT POWDER FREE EXAMINATION GLOVES (..., manufactured by Wembley Rubber Products (M) Sdn Bhd. The device is a Class 1 General Hospital device with product code LYY cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K935852 · Wembley Rubber Products (M) Sdn Bhd · General Hospital
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Mar 1994
Decision
89d
Days
Class 1
Risk

K935852 is an FDA 510(k) clearance for the COMFIT POWDER FREE EXAMINATION GLOVES (HYPOALLERGENIC). Classified as Latex Patient Examination Glove (product code LYY), Class I - General Controls.

Submitted by Wembley Rubber Products (M) Sdn Bhd (Malaysia, MY). The FDA issued a Cleared decision on March 7, 1994 after a review of 89 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 Wembley Rubber Products (M) Sdn Bhd devices

FDA 510(k) Submission Details - K935852

510(k) Number K935852 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 1993
Decision Date March 07, 1994
Days to Decision 89 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
40d faster than avg
Panel avg: 129d · This submission: 89d
Pathway characteristics
Predicate-based equivalence.

LYY Device Classification - Class 1, General Controls

Product Code LYY Latex Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Latex Patient Examination Glove Is A Disposable Device Made Of Natural Rubber Latex 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 - LYY Latex Patient Examination Glove

All 912
Devices cleared under the same product code (LYY) and FDA review panel - the closest regulatory comparables to K935852.
PATIENT EXAMINATION GLOVES
K935256 · Comfort Rubber Gloves Industries Sdn. Bhd. · Mar 1994
ULTAR-SHIELD
K932702 · Medical Resources International, Inc. · Mar 1994
EXTRA CARE
K934721 · Genting Sempurna Sdn. Bhd. · Mar 1994
POWDER FREE LATEX EXAMINATION GLOVES
K926426 · Dah Lee Investments, Ltd. · Feb 1994
POWDER FREE LATEX EXAMINATION GLOVES
K934409 · Sjs Supreme, Inc. · Feb 1994
LATEX EXAMINATION GLOVES
K930655 · Pushpaman Processors, Div. Kanjur Bleaching Co. PV · Feb 1994