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510(k) Data Aggregation

    K Number
    K172678

    Validate with FDA (Live)

    Manufacturer
    Date Cleared
    2017-11-24

    (80 days)

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

    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 patient and examiner

    Device Description

    Thermoplastic Elastomer Examination (TPE) Glove

    AI/ML Overview

    The provided text is related to the FDA's clearance of a medical device, specifically a "Thermoplastic Elastomer Examination (TPE) Glove," as described in K172678.

    However, the document is a 510(k) clearance letter and does not contain the detailed information requested regarding acceptance criteria and the study that proves the device meets those criteria, as typically found in a clinical study report or a more comprehensive technical document.

    The 510(k) clearance process primarily focuses on demonstrating substantial equivalence to a predicate device, rather than detailed performance evaluations with specific acceptance criteria and study designs in the way you've outlined for AI or diagnostic devices.

    Therefore, I cannot provide the requested information from this document. The information you're asking for (e.g., sample size, expert qualifications, adjudication methods, MRMC studies, standalone performance, training set details) is typical for the evaluation of AI/ML-based medical devices or complex diagnostic systems, not for a Class I patient examination glove which is typically evaluated based on manufacturing quality, integrity, and barrier properties, often using standardized test methods.

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