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510(k) Data Aggregation

    K Number
    K993452
    Date Cleared
    1999-12-20

    (68 days)

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

    GREEN POWDERED LATEX EXAMINATION GLOVES

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

    Powdered Green Latex Examination Gloves (vith minimum length of 280mm) are worn on the hands of Health care and similar personnel to give an additional protection until the arm to prevent contamination between health care personnel and the patient especially for the Emergency Medical Service.

    Device Description

    Powdered Green Latex Examination Glove

    AI/ML Overview

    This document is a 510(k) premarket notification letter from the FDA regarding "Green Powdered Latex Examination Gloves." It confirms that the device is substantially equivalent to legally marketed predicate devices.

    This document does not contain information about acceptance criteria, device performance studies, or clinical trial details. It is a regulatory approval letter based on "substantial equivalence" to existing devices, not a report on a new device's performance against specific criteria.

    Therefore, I cannot provide the requested information from this text. The questions you've asked typically relate to detailed technical or clinical studies supporting a device's efficacy and safety, which are not present in this regulatory correspondence.

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