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510(k) Data Aggregation

    K Number
    K110966
    Date Cleared
    2011-07-21

    (106 days)

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

    Powdered Vinyl Patient Examination Gloves, Light Yellow Color is a non-sterile disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.

    Device Description

    Powdered Vinyl Patient Examination Gloves, Light Yellow Color that meets all of the requirements of ASTM standard D 5250-06e1.

    AI/ML Overview

    The provided text describes a 510(k) summary for "Powdered Vinyl Patient Examination Gloves, Light Yellow Color." This is a medical device that falls under the category of general hospital devices, specifically patient examination gloves.

    The text does not describe an AI/ML powered device, nor does it involve any studies related to human readers, AI assistance, or complex diagnostic tasks. The "acceptance criteria" and "study" described in the document are for basic physical, chemical, and biological properties of the gloves, not for an AI algorithm.

    Therefore, I cannot extract the information required for the requested table and parameters related to an AI/ML device. The document pertains to a much simpler Class I medical device.

    Here's a breakdown of why this document doesn't fit the request and what information can be extracted:

    • No AI/ML Component: The device is a physical product (gloves), not a software or AI-driven system.
    • No "Ground Truth" for AI: Concepts like expert consensus, pathology, or outcomes data as "ground truth" are irrelevant for examination gloves.
    • No "Readers" or "Adjudication": There are no human readers or AI algorithms being evaluated in a diagnostic context.
    • No "Sample Size for Test/Training Set" in AI Sense: The phrase "sample size" in this document refers to the quantity of gloves tested for physical properties (e.g., freedom from pinholes), not data points for an AI model.
    • No "Effect Size of Human Readers Improve with AI": This is completely unrelated to the device described.

    What can be extracted related to "acceptance criteria" from the provided text for this specific device:

    The "acceptance criteria" are essentially the relevant ASTM standards and FDA regulations that the gloves must meet. The "device performance" is stated as "Meets" for all these criteria.

    Table of Acceptance Criteria and Reported Device Performance (as per the document):

    Acceptance Criteria / CharacteristicReference StandardReported Device Performance
    DimensionASTM standard D 5250-06 elMeets
    Physical PropertiesASTM standard D 5250-06 elMeets
    Freedom from pinholes21 CFR 800.20Meets
    Powder AmountASTM standard D 5250-06 el and D6124-06Meets (
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