Cleared Traditional

K945490 - LATEX EXAMINATION GLOVE

K945490 is an FDA 510(k) clearance for LATEX EXAMINATION GLOVE, manufactured by Masif Healthcare Products Sdn. Bhd.. The device is a Class 1 General Hospital device with product code LYY cleared through the Traditional 510(k) pathway after a 30-day FDA review.

K945490 · Masif Healthcare Products Sdn. Bhd. · General Hospital
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Dec 1994
Decision
30d
Days
Class 1
Risk

K945490 is an FDA 510(k) clearance for the LATEX EXAMINATION GLOVE. Classified as Latex Patient Examination Glove (product code LYY), Class I - General Controls.

Submitted by Masif Healthcare Products Sdn. Bhd. (Malaysia, MY). The FDA issued a Cleared decision on December 8, 1994 after a review of 30 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 Masif Healthcare Products Sdn. Bhd. devices

FDA 510(k) Submission Details - K945490

510(k) Number K945490 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 08, 1994
Decision Date December 08, 1994
Days to Decision 30 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
99d faster than avg
Panel avg: 129d · This submission: 30d
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 294
Devices cleared under the same product code (LYY) and FDA review panel - the closest regulatory comparables to K945490.
SCIPOTEX
K943868 · Wembley Rubber Products (M) Sdn Bhd · Feb 1995
POWDERFREE LATEX EXAMINATION GLOVE
K945247 · Sri Johani Sdn. Bhd. · Jan 1995
LATEX MEDICAL GLOVE
K943900 · Johnson & Johnson Medical, Inc. · Dec 1994
COMFIT BLUE POWDERED EXAMINATION GLOVES
K936268 · Wembley Rubber Products (M) Sdn Bhd · Dec 1994
COMFIT
K944140 · Wembley Rubber Products (M) Sdn Bhd · Dec 1994
COMFIT EXAMINATION GLOVES, POWDER FREE, HYPOALLERGENIC
K942947 · Wembley Rubber Products (M) Sdn Bhd · Nov 1994