Cleared Traditional

K992219 - POWDERED LATEX STERILE SURGICAL GLOVES

K992219 is an FDA 510(k) clearance for POWDERED LATEX STERILE SURGICAL GLOVES, manufactured by Tg Medical Sdn. Bhd.. The device is a Class 1 General Hospital device with product code KGO cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K992219 · Tg Medical Sdn. Bhd. · General Hospital
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Jul 1999
Decision
29d
Days
Class 1
Risk

K992219 is an FDA 510(k) clearance for the POWDERED LATEX STERILE SURGICAL GLOVES. Classified as Surgeon's Gloves (product code KGO), Class I - General Controls.

Submitted by Tg Medical Sdn. Bhd. (Klang, Selangor D.E., MY). The FDA issued a Cleared decision on July 30, 1999 after a review of 29 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4460 - 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 Tg Medical Sdn. Bhd. devices

FDA 510(k) Submission Details - K992219

510(k) Number K992219 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1999
Decision Date July 30, 1999
Days to Decision 29 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
100d faster than avg
Panel avg: 129d · This submission: 29d
Pathway characteristics
Predicate-based equivalence.

KGO Device Classification - Class 1, General Controls

Product Code KGO Surgeon's Gloves
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4460
Definition A Surgeon's Glove Is A Disposable Device Made Of Natural Rubber Latex Or Synthetic Polymers That May Or May Not Bear Powder To Facilitate Donning, And It Is Intended To Be Worn On The Hands, Usually In Surgical Settings, 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 - KGO Surgeon's Gloves

All 272
Devices cleared under the same product code (KGO) and FDA review panel - the closest regulatory comparables to K992219.
LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE)
K991950 · La Glove (M) Sdn. Bhd. · Aug 1999
LAGLOVE POWDER FREE LATEX SURGICAL GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
K992019 · La Glove (M) Sdn. Bhd. · Aug 1999
LAGLOVE POWDERED LATEX SURGICAL GLOVES WITH PROTEIN CONTENT LABELING CLAIM (150 MICROGRAMS OR LESS)
K992018 · La Glove (M) Sdn. Bhd. · Jul 1999
ULTRAFREE THICK STERILE LATEX POWDER-FREE SURGICAL GLOVES
K991992 · Allegiance Healthcare Corp. · Jul 1999
BRIGHTWAY BRAND NITRILE SURGICAL GLOVES - STERILE (POWDERED)
K991940 · Brightway Holdings Sdn. Bhd. · Jul 1999
BRIGHTWAY BRAND NITRILE SURGICAL GLOVES - STERILE (POWDER-FREE)
K991939 · Brightway Holdings Sdn. Bhd. · Jul 1999