Cleared Traditional

K935870 - DEXTREN POWDER FREE HYPOALLERG GLOVES W...

K935870 is an FDA 510(k) clearance for DEXTREN POWDER FREE HYPOALLERG GLOVES W..., manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device is a Class 1 General Hospital device with product code KGO cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K935870 · Bd Becton Dickinson Vacutainer Systems Preanalytic · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1994
Decision
74d
Days
Class 1
Risk

K935870 is an FDA 510(k) clearance for the DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS. Classified as Surgeon's Gloves (product code KGO), Class I - General Controls.

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Franklin Lake, US). The FDA issued a Cleared decision on February 18, 1994 after a review of 74 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 Bd Becton Dickinson Vacutainer Systems Preanalytic devices

FDA 510(k) Submission Details - K935870

510(k) Number K935870 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 06, 1993
Decision Date February 18, 1994
Days to Decision 74 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 129d · This submission: 74d
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 188
Devices cleared under the same product code (KGO) and FDA review panel - the closest regulatory comparables to K935870.
COMFIT
K935464 · Wembley Rubber Products (M) Sdn Bhd · May 1994
MAXXUS ORTHOPAEDIC LATEX SURGICAL GLOVES
K935227 · Johnson & Johnson Medical, Inc. · Mar 1994
DEXTREN(TM) POWDER FREE HYPOALLERGENIC GLOVES
K935869 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1994
B-D(R) CHALLENGE POWDER FREE SYNTHETIC SURG GLOVES
K933062 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jan 1994
INTEGRON SURGICAL GLOVES
K924071 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Nov 1993
ULTRALON POWDERFREE SURGICAL GLOVES
K915218 · Johnson & Johnson Medical, Inc. · Dec 1992