Cleared Traditional

K962837 - NULIFE

K962837 is an FDA 510(k) clearance for NULIFE, manufactured by Med-Tech Rubber & Engineering Industries. The device is a Class 1 General Hospital device with product code KGO cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K962837 · Med-Tech Rubber & Engineering Industries · General Hospital
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Oct 1996
Decision
85d
Days
Class 1
Risk

K962837 is an FDA 510(k) clearance for the NULIFE. Classified as Surgeon's Gloves (product code KGO), Class I - General Controls.

Submitted by Med-Tech Rubber & Engineering Industries (Sussex Rad, Yculla,, IN). The FDA issued a Cleared decision on October 2, 1996 after a review of 85 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 Med-Tech Rubber & Engineering Industries devices

FDA 510(k) Submission Details - K962837

510(k) Number K962837 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 09, 1996
Decision Date October 02, 1996
Days to Decision 85 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
44d faster than avg
Panel avg: 129d · This submission: 85d
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 311
Devices cleared under the same product code (KGO) and FDA review panel - the closest regulatory comparables to K962837.
ULTREX POWDER-FREE SURGICAL GLOVES/ULTREX POWDER-FREE SURGICAL GLOVES WITH LOW PROTEIN CLAIM
K964980 · Maxxim Medical · Mar 1997
DEXTREN CLEAR POWDER-FREE HYPOALLERGENIC SURGICAL GLOVES
K962813 · Maxxim Medical · Jan 1997
STERILE LATEX SURGICAL, SOLD UNDER BRAND NAMES SAVACARE AND ROGUMED
K962724 · Sonnheim Medikal GmbH · Oct 1996
MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES
K962986 · Johnson & Johnson Medical, Inc. · Sep 1996
MICRO-TOUCH POWDER FREE LATEX SURGICAL GLOVES
K961632 · Johnson & Johnson Medical, Inc. · Jul 1996
NEOLON NEOPRENE SURGICAL GLOVES
K954325 · Maxxim Medical · May 1996