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510(k) Data Aggregation

    K Number
    K994246
    Manufacturer
    Date Cleared
    2000-01-31

    (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 medical glove is wom on the hand of healthcare and similar personnel to prevent contamination between health care personnel and the patient.

    Device Description

    OmniGrace Nitrile, Blue, Examination Glove, Powder Free, Polymer Coated.

    AI/ML Overview

    This document is a 510(k) premarket notification decision letter from the FDA to OmniGrace (Thailand) Ltd. regarding their Nitrile, Blue, Powder-Free, Polymer Coated Patient Examination Glove. The letter indicates that the device has been found substantially equivalent to devices marketed prior to May 28, 1976.

    Unfortunately, this document does not contain the information requested regarding acceptance criteria and the study that proves the device meets those criteria. The provided text is a regulatory approval letter and an "Indications for Use Statement," not a study report or a detailed description of performance testing.

    Therefore, I cannot provide the requested table or answer the specific questions about sample size, expert involvement, adjudication, MRMC studies, standalone performance, ground truth, or training set details. This information would typically be found in the 510(k) submission itself, or in subsequent test reports, which are not part of this document.

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