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510(k) Data Aggregation

    K Number
    K112012
    Date Cleared
    2012-03-21

    (252 days)

    Product Code
    Regulation Number
    880.6250
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Non-Sterile, Powder-Free, Nitrile Examination Gloves Blue is a disposable device intended for Medical Purposes that is worn on the examiners hand to prevent contamination between patient and examiner.

    Device Description

    Non-Sterile, Powder-Free, Nitrile Examination Gloves Blue. A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between the patient and the examiner.
    Summary of Technological Characteristics:
    Cuff: Beaded
    Material: Nitrile
    Powder Residue: Maximum 2mg/glove
    Quality Assurance: In compliance with ASTM D6319-10, ISO 2859-1, manufactured under ISO9001:2008 and ISO 13485:2003
    Physical Properties:
    Overall Length: 240 mm minimum
    Width: 95 mm minimum (for medium glove)
    Thickness: .05 mm minimum
    BEFORE AGING: Tensile Strength: 14.0 Mpa minimum, Ultimate Elongation: 500% minimum
    AFTER AGING: Tensile Strength: 14.0 Mpa minimum, Ultimate Elongation: 400% minimum
    Special Properties: None
    Packaging: 150 pcs per dispenser box, 10 boxes per case, 1,500 gloves per case
    Sizes: XS — XL

    AI/ML Overview

    This document describes the acceptance criteria and performance of "Non-Sterile, Powder-Free, Nitrile Examination Gloves Blue" (K112012), not an AI device. Therefore, many of the requested sections related to AI device studies (e.g., sample size for test set, ground truth experts, MRMC studies, standalone performance, training set details) are not applicable.

    Here's the available information based on the provided text, adapted to the closest relevant categories:

    1. Table of Acceptance Criteria and Reported Device Performance

    CriteriaAcceptance CriteriaReported Device Performance
    Powder ResidueMaximum 2mg/gloveNot explicitly stated, but implies meeting this
    Quality AssuranceIn compliance with ASTM D6319-10, ISO 2859-1, ISO9001:2008, ISO 13485:2003Stated as being in compliance
    Dimensions (Inspection)AQL 4.0 (S-2 level)Not explicitly stated as pass/fail, but implies meeting this
    Physical Properties (Inspection)AQL 4.0 (S-2 level)Not explicitly stated as pass/fail, but implies meeting this
    Water Tight Test (1000ml, Inspection)AQL 1.5 (G-1 level)Met both before and after aging
    Visual Major Defects (Inspection)AQL 1.5 (G-1 level)Not explicitly stated as pass/fail, but implies meeting this
    Visual Minor Defects (Inspection)AQL 2.5 (G-1 level)Not explicitly stated as pass/fail, but implies meeting this
    Overall Length240 mm minimumNot explicitly stated as a measured value, but implies meeting this
    Width (medium glove)95 mm minimumNot explicitly stated as a measured value, but implies meeting this
    Thickness0.05 mm minimumNot explicitly stated as a measured value, but implies meeting this
    BEFORE AGING
    Tensile Strength14.0 Mpa minimum14.0 Mpa minimum
    Ultimate Elongation500% minimum500% minimum
    AFTER AGING
    Tensile Strength14.0 Mpa minimum14.0 Mpa minimum
    Ultimate Elongation400% minimum400% minimum
    Protein Labeling Claim Level
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