Cleared Traditional

K962539 - GANTEX MODEL NSG-75PF

K962539 is an FDA 510(k) clearance for GANTEX MODEL NSG-75PF, manufactured by American Pro Latex, Inc.. The device is a Class 1 General Hospital device with product code KGO cleared through the Traditional 510(k) pathway after a 381-day FDA review.

K962539 · American Pro Latex, Inc. · General Hospital
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Jul 1997
Decision
381d
Days
Class 1
Risk

K962539 is an FDA 510(k) clearance for the GANTEX MODEL NSG-75PF. Classified as Surgeon's Gloves (product code KGO), Class I - General Controls.

Submitted by American Pro Latex, Inc. (Chicago, US). The FDA issued a Cleared decision on July 14, 1997 after a review of 381 days - an unusually long review period, suggesting complex equivalence evaluation.

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: Standard predicate-based submission. Elevated predicate reliance profile. 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.

View all American Pro Latex, Inc. devices

FDA 510(k) Submission Details - K962539

510(k) Number K962539 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 28, 1996
Decision Date July 14, 1997
Days to Decision 381 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
252d slower than avg
Panel avg: 129d · This submission: 381d
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 351
Devices cleared under the same product code (KGO) and FDA review panel - the closest regulatory comparables to K962539.
DIGIFLEX SURGICAL GLOVES
K972277 · Hms Services, Inc. · Oct 1997
PURE ADVANTAGE NITRILE HYPOALLERGENIC SURGICAL GLOVE
K972009 · Tillotson Healthcare Corp. · Sep 1997
UNIJECT SURGICAL GLOVES
K970160 · Uniject Gloves , Ltd. · Jul 1997
PURE ADVANTAGE POWDER FREE NITRILE HYPOALLERGENIC SURGICAL GLOVE
K971945 · Tillotson Healthcare Corp. · Jul 1997
POWDER-FREE DURAPRENE STERILE SYNTHETIC SURGICAL GLOVES
K971381 · Allegiance Healthcare Corp. · Jul 1997
EUDERMIC HYPOALLERGENIC SURGICAL GLOVES/EUDERMIC SURGICAL GLOVES (VARIOUS)
K964440 · Maxxim Medical · Apr 1997