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510(k) Data Aggregation

    K Number
    K051317
    Date Cleared
    2005-06-20

    (31 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

    This glove is disposable and intended for medical purpose that is worn on the examiner's hand to prevent contamination between patient and examiner.

    Device Description

    Polymer Coated Powder Free Nitrile Examination Gloves, Blue, Green and White color.

    AI/ML Overview

    The provided document is an FDA 510(k) Pre-market Notification letter for Polymer Coated Powder Free Nitrile Examination Gloves. This type of document is a regulatory approval and does not contain the information requested regarding acceptance criteria and a study proving device performance in the context of an AI/ML-based medical device.

    The questions you've asked are typical for studies evaluating the performance of algorithms or diagnostic devices (often involving AI/ML), where there's a need to establish sensitivity, specificity, accuracy, and compare to a ground truth established by experts.

    This document, however, pertains to a physical medical device (examination gloves) and focuses on substantial equivalence to a predicate device, as per the FDA 510(k) process for Class I devices. The "performance" for such a device is typically assessed through physical properties and safety standards, rather than diagnostic accuracy metrics.

    Therefore, I cannot extract the requested information from this document.

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