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510(k) Data Aggregation

    K Number
    K032745
    Date Cleared
    2003-10-17

    (43 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

    Shanghai Giantmax Plastic Products Powdered Clear Vinyl Examination Glove

    AI/ML Overview

    The provided text is a 510(k) premarket notification letter for a medical device, specifically a "Shanghai Giantmax Powdered Clear Vinyl Examination Glove." This document is a regulatory approval letter from the FDA and does not contain information about acceptance criteria or a study proving the device meets those criteria, as typically found in clinical trial reports or technical performance reports.

    The letter states that the FDA reviewed the premarket notification and determined the device is substantially equivalent to legally marketed predicate devices for the indicated use. This determination is based on the device meeting the general controls provisions of the Federal Food, Drug, and Cosmetic Act.

    Therefore, I cannot provide the requested information based on the provided text. The document does not describe:

    1. A table of acceptance criteria and reported device performance.
    2. Sample size or data provenance for a test set.
    3. Number or qualifications of experts used for ground truth.
    4. Adjudication method for a test set.
    5. Details of a multi-reader multi-case (MRMC) comparative effectiveness study or effect size.
    6. Results of a standalone (algorithm-only) performance study.
    7. Type of ground truth used.
    8. Sample size for a training set.
    9. How ground truth for a training set was established.

    This document focuses on regulatory compliance and substantial equivalence rather than detailed performance study results.

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