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510(k) Data Aggregation

    K Number
    K000090
    Date Cleared
    2000-02-10

    (28 days)

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

    GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K990228
    Date Cleared
    1999-02-19

    (25 days)

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

    GUTHRIE PRIME POWDER-FREE

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

    Powder-free Patient Examination glove is a disposable device which is primarily Intended for modition between patient and patient and examiner's hand or finger to prevent Intended for modition between patient and examiner.

    Device Description

    Powder-Free Latex Examination Trade Name: Gloves with 50 Micrograms or Less of Total Water Extractable Protein Per Gram

    AI/ML Overview

    The provided text is a letter from the FDA regarding a Guthrie Prime Powder-Free Latex Examination Glove. This document is a 510(k) premarket notification and primarily focuses on the regulatory approval for this medical device, asserting its substantial equivalence to previously marketed devices.

    Based on the content, this document does not contain the information needed to describe acceptance criteria and a study proving a device meets them in the context of the requested details (e.g., AI performance, expert ground truth, sample sizes for test/training sets, MRMC studies). The device mentioned is a physical product (latex gloves), not a software or AI-driven diagnostic device that would typically have such performance criteria.

    Therefore, I cannot fulfill your request using the provided text. The document is about a regulatory approval for a physical medical device, not a performance study as described in your prompt.

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