Cleared Traditional

K933062 - B-D CHALLENGE POWDER FREE SYNTHETIC SUR...

K933062 is an FDA 510(k) clearance for B-D CHALLENGE POWDER FREE SYNTHETIC SUR..., 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 214-day FDA review.

K933062 · Bd Becton Dickinson Vacutainer Systems Preanalytic · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1994
Decision
214d
Days
Class 1
Risk

K933062 is an FDA 510(k) clearance for the B-D(R) CHALLENGE POWDER FREE SYNTHETIC SURG GLOVES. Classified as Surgeon's Gloves (product code KGO), Class I - General Controls.

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Franklin Lakes, US). The FDA issued a Cleared decision on January 31, 1994 after a review of 214 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. 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 Bd Becton Dickinson Vacutainer Systems Preanalytic devices

FDA 510(k) Submission Details - K933062

510(k) Number K933062 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1993
Decision Date January 31, 1994
Days to Decision 214 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
85d slower than avg
Panel avg: 129d · This submission: 214d
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 K933062.
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
DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS
K935870 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1994
INTEGRON SURGICAL GLOVES
K924071 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Nov 1993
ULTRALON POWDERFREE SURGICAL GLOVES
K915218 · Johnson & Johnson Medical, Inc. · Dec 1992
PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER)
K922515 · Wembley Rubber Products (M) Sdn Bhd · Nov 1992