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510(k) Data Aggregation

    K Number
    K983721
    Date Cleared
    1998-12-07

    (46 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 purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.

    Device Description

    Polymer-Coated, Powder-Free, Latex Patient Examination Glove

    AI/ML Overview

    The provided document is a 510(k) premarket notification letter from the FDA regarding a Polymer-Coated, Powder-Free, Latex Patient Examination Glove. This document approves the market entry of a medical device and therefore, does not contain information about acceptance criteria or a study proving that the device meets those criteria.

    The document discusses:

    • The FDA's review and determination of substantial equivalence for the device.
    • The regulatory classification of the device (Class I).
    • General controls provisions of the Act that apply to the device.
    • Contact information for further inquiries regarding labeling regulations and promotion/advertising.
    • The intended use of the device: "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."

    To answer your specific questions, information about acceptance criteria, study details, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, and ground truth establishment would typically be found in the 510(k) submission document itself, not in the FDA's response letter. The FDA letter is a confirmation of clearance based on the information provided in the submission.

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