Cleared Traditional

K102500 - STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING

K102500 is an FDA 510(k) clearance for STERILE NEOPRENE POWDER-FREE SURGICAL G..., manufactured by Cardinal Health, Inc.. The device is a Class 1 General Hospital device with product code KGO cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K102500 · Cardinal Health, Inc. · General Hospital
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Nov 2010
Decision
64d
Days
Class 1
Risk

K102500 is an FDA 510(k) clearance for the STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING. Classified as Surgeon's Gloves (product code KGO), Class I - General Controls.

Submitted by Cardinal Health, Inc. (Waukegan, US). The FDA issued a Cleared decision on November 4, 2010 after a review of 64 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 Cardinal Health, Inc. devices

FDA 510(k) Submission Details - K102500

510(k) Number K102500 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 01, 2010
Decision Date November 04, 2010
Days to Decision 64 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
65d faster than avg
Panel avg: 129d · This submission: 64d
Pathway characteristics
Predicate-based equivalence. Third-party reviewed.

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 Consultant

Underwriters Laboratories, Inc.
NED DEVINE

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - KGO Surgeon's Gloves

All 368
Devices cleared under the same product code (KGO) and FDA review panel - the closest regulatory comparables to K102500.
STERILE POLYISOPRENE POWDER-FREE SURGICAL GLOVES TESTED FOR USE WITH CHEMOTHERAPY DRUG
K110272 · Cardinal Health, Inc. · Jun 2011
STERILE LATEX POWDER FREE SURGICAL GLOVES WITH HYDROGEL COATING
K111015 · Cardinal Health, Inc. · May 2011
BIOGEL ORTHOPRO INDICATOR UNDERGLOVE
K101163 · Molnlycke Health Care USA · Nov 2010
PROTEGRITY SMT LATEX SURGICALGLOVES
K101811 · Cardinal Health, Inc. · Oct 2010
SUR-G GLOV AND MAXITEX
K102119 · Terang Nusa Sdn Bhd · Aug 2010
POWDER-FREE, NATURAL COLOR, LATEX SURGICAL GLOVE, STERILE
K101102 · Best Putra Gloves Sdn Bhd · Jul 2010

FDA 510(k) Resources - General Hospital

Additional regulatory intelligence related to this FDA 510(k) submission, including predicate strategy, review pathways and device classification guidance.