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510(k) Data Aggregation

    K Number
    K990420
    Date Cleared
    1999-03-29

    (47 days)

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

    LAGLOVE BRAND NITRILE EXAMINATION GLOVE (POWDER FREE)

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

    Laglove™ Brand Nitrile Examination Glove (Powder Free) is a disposable patient examination glove which is worn on the hand of the examiner to prevent contamination between patient and examiner.

    Device Description

    Laglove™ Brand Nitrile Examination Glove (Powder Free)

    AI/ML Overview

    The provided document is a 510(k) premarket notification letter from the FDA regarding "Laglove™ Brand Nitrile Examination Glove (Powder-Free)". This type of document is a regulatory approval for a medical device and does not contain the detailed technical study information requested in your prompt.

    Therefore, I cannot provide the specific information about:

    1. A table of acceptance criteria and the reported device performance
    2. Sample sizes used for the test set and data provenance
    3. Number of experts used to establish ground truth and their qualifications
    4. Adjudication method
    5. Multi-reader multi-case (MRMC) comparative effectiveness study results
    6. Standalone performance study details
    7. Type of ground truth used
    8. Sample size for the training set
    9. How ground truth for the training set was established

    This document only confirms that the FDA has determined the device is substantially equivalent to legally marketed predicate devices. It states the indications for use are as "a disposable patient examination glove [worn] on the hand of the examiner to prevent contamination between patient and examiner." The regulatory class is I, and the product code is LZA.

    To obtain the information you're looking for, you would typically need access to the actual 510(k) submission document, which would include performance data, test methods, and potentially a summary of clinical or non-clinical studies if required for that specific device type.

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