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510(k) Data Aggregation

    K Number
    K992681
    Date Cleared
    1999-12-16

    (128 days)

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

    PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE

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

    A patient Examination Powder glove sterile 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.
    A patient Examination Powder-Free Chlorinated glove sterile 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

    Patient Latex Examination Glove Powdered & Powder-Free, Sterile

    AI/ML Overview

    This document is a 510(k) premarket notification decision letter from the FDA for medical examination gloves and does not contain information about acceptance criteria or a study proving device performance in the way typically expected for an AI/ML medical device.

    The information provided in the document pertains to the regulatory clearance of a physical medical device (latex examination gloves) based on substantial equivalence to a predicate device, not on algorithmic performance or clinical study outcomes involving AI.

    Therefore, I cannot extract the requested information (acceptance criteria table, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth types, or training set details) from this document. The concepts are not applicable to the content of the provided text.

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