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510(k) Data Aggregation

    K Number
    K180644
    Manufacturer
    Date Cleared
    2018-08-10

    (151 days)

    Product Code
    Regulation Number
    880.6250
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    Nitrile Powder Free Examination Gloves with Colloidal Oatmeal - Lemon Green

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Nitrile Powder Free Examination Glove with Colloidal Oatmeal - Lemon Green 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.

    Device Description

    Nitrile Powder Free Examination Glove with Colloidal Oatmeal - Lemon Green

    AI/ML Overview

    The provided text describes an FDA 510(k) clearance for "Nitrile Powder Free Examination Gloves with Colloidal Oatmeal - Lemon Green." This document is a regulatory approval for a medical device (patient examination gloves). It does NOT contain information about an AI/ML-based medical device, a study proving device performance against acceptance criteria for an AI/ML system, or details about the development and testing of an AI algorithm.

    Therefore, I cannot extract the requested information regarding acceptance criteria, study details, sample sizes, expert ground truth, adjudication methods, MRMC studies, standalone performance, training set details, or ground truth establishment the way you would for an AI/ML device.

    The information in the provided text relates to:

    • Device Name: Nitrile Powder Free Examination Gloves with Colloidal Oatmeal - Lemon Green
    • Regulation Number: 21 CFR 880.6250 (Patient Examination Glove)
    • Regulatory Class: Class I
    • Product Code: LZA
    • Indications for Use: Non-sterile disposable device intended for medical purpose, worn on the examiner's hand to prevent contamination between patient and examiner.
    • Use Type: Over-The-Counter Use

    This is a clearance for a physical medical device, not a software or AI/ML-based device. If you have a different document describing an AI/ML device and its validation study, please provide that text.

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