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510(k) Data Aggregation

    K Number
    K140890
    Date Cleared
    2014-07-24

    (107 days)

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

    The Nitrile Powder Free Examination Glove - Cobalt Blue (CBLU) is a non - sterile disposable device intended for medical purpose that is worn on the examiner's hand to prevent contamination between patient and examiner
    The Nitrile Powder Free Examination Glove - Dark Violet Blue (DVBU) is a non - sterile disposable device intended for medical purpose that is worn on the examiner's hand to prevent contamination between patient and examiner
    The Nitrile Powder Free Examination Glove - Dawn Blue is a non - sterile disposable device intended for medical purpost that is worn on the examiner's hand to prevent contamination between patient and examiner
    The Nittile Powder Free Examination Glove - White is a non - sterile disposable device intended for medical puppose that is wom on the examiner's hand to prevent contamination between patient and examiner

    Device Description

    Not Found

    AI/ML Overview

    This document is a 510(k) premarket notification decision letter from the FDA for several types of Nitrile Powder Free Examination Gloves. It primarily addresses the substantial equivalence of these gloves to legally marketed predicate devices.

    Key takeaway: This document is an administrative approval of a medical device (gloves) and does not contain information about acceptance criteria or performance studies as typically described for software or AI/ML devices. The information requested in the prompt, such as sample sizes for test/training sets, ground truth establishment, expert qualifications, and AI-specific study details (MRMC, standalone performance, effect size), is not applicable to this type of regulatory submission for examination gloves.

    The approval is based on the device being "substantially equivalent" to predicate devices, meaning it has the same intended use and technological characteristics, or if it has different technological characteristics, it does not raise different questions of safety and effectiveness.

    Therefore, I cannot extract the requested information from this document because it is not present. The document focuses on regulatory compliance for a Class I medical device (patient examination glove), not on the performance analysis of a new or AI-powered technology.

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