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510(k) Data Aggregation

    K Number
    K990299
    Date Cleared
    1999-03-29

    (56 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

    A PATIENT EXAMINATION GLOVE IS A DISPOSABLE DEVICE INTENDED FOR MEDICAL PURPOSE THAT IS WORN ON THE EXAMINER'S HAND OR FINGER TO PREVENT CONTAMINATION BETWEEN PATIENT AND EXAMINER.

    Device Description

    POWDER FREE COPOLYMER NITRILE MEDICAL EXAMINATION GLOVE, COLORED.

    AI/ML Overview

    This looks like a letter from the FDA regarding a 510(k) premarket notification for examination gloves, not an AI/ML device or a study related to acceptance criteria.

    The document discusses:

    • K990299 Powder-Free Copolymer Nitrile Medical Examination Gloves.
    • The FDA's determination that the device is substantially equivalent to a predicate device.
    • General controls provisions of the Act (annual registration, listing of devices, good manufacturing practice, labeling, etc.).
    • Information on labeling regulations, promotion and advertising, and other responsibilities under the Act.
    • The "Indications for Use" statement for the gloves, which states they are a disposable device intended for medical purposes to prevent contamination between patient and examiner.

    Therefore, the requested information about acceptance criteria, study details, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth, and training data for an AI/ML device cannot be extracted from this document, as it is completely unrelated to such a device or study.

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