Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K061551
    Date Cleared
    2006-08-24

    (80 days)

    Product Code
    Regulation Number
    880.6250
    Reference & Predicate Devices
    Predicate For
    N/A
    Why did this record match?
    Reference Devices :

    K924356

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Powder Free Latex Examination Glove is a disposable device made of natural rubber latex that may bear a trace amount of glove powder and is intended to be worn on hands or finger(s) for medical purposes to provide a barrier.against potentially infectious materials and other contaminants.

    Device Description

    The Powder Free Latex Examination Gloves. Natural or Blue Colour and with Protein Content Labeling Claim is equivalent to the exiting model, i.e. Latex Patient Examination Gloves. Powder Free which had submitted and cleared under 510(k) number K924356.

    The differences in this submission are:

    • With or without colour additive upon customers` preference or request. a)
    • With protein content labeling claim, i.e. "This latex glove contains 50 micrograms or b) less of total water extractable protein per gram``.
    AI/ML Overview

    The provided document is a 510(k) summary for a medical device: "Powder Free Latex Examination Gloves, Natural or Blue Colour and with Protein Content Labeling Claim (50 Micrograms or Less)". This type of submission is for demonstrating substantial equivalence to a legally marketed predicate device, not for proving the safety and effectiveness of a novel device through extensive clinical trials. Therefore, many of the typical clinical study criteria (like sample size for test set, number of experts, adjudication methods, MRMC studies, standalone AI performance, and training set information) are not applicable or not detailed in this type of regulatory filing.

    The acceptance criteria are primarily based on established ASTM standards and FDA regulations for patient examination gloves. The "study" proving the device meets these criteria is a series of tests against these standards.

    Here's a breakdown based on the information provided:


    1. Table of Acceptance Criteria and Reported Device Performance

    CharacteristicsAcceptance Criteria (Standards)Reported Device PerformanceOutcome
    Palm Width (Medium)ASTM D 357891 - 92 mmMeets
    Length (Medium)ASTM D 3578285 - 292 mmMeets
    Finger Thickness (Medium)ASTM D 35780.38 - 0.40 mmMeets
    Palm Thickness (Medium)ASTM D 35780.35 - 0.37 mmMeets
    Tensile Strength (Unaged)ASTM D 357822.88 - 30.87 MPaMeets
    Tensile Strength (Aged)ASTM D 357821.05 - 27.60 MPaMeets
    Freedom from pinholesASTM D 3578 & FDA 21 CFR 800.20 (Acceptable Quality Level 1.5)0/125 (meaning 0 failures out of 125 tested, which meets 1/125)Meets
    Visual Inspection - Major defectsIn-House Specification (AQL 2.5)1/125Meets
    Visual Inspection - Minor defectsIn-House Specification (AQL 4.0)1/125Meets
    Powder ResidualASTM D 3578 & ASTM D 6124 (
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1