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510(k) Data Aggregation

    K Number
    K102880
    Date Cleared
    2010-11-19

    (50 days)

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

    BRIGHTWAY TM BRAND NITRILE EXAMINATION GLOVES, POWDER FREE, NON-STERILE. (GREY COLOR)

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

    Brightway TM Brand Nitrile Examination Gloves, Powder Free, Non - Sterile (Grey Color) is a patient examination glove is a disposable device intended for medical purpose worn on the examiners hand or finger to prevent contamination between patient and examiner.

    Device Description

    Brightway ™ Brand Nitrile Examination Gloves, Powder Free, Non-Sterile. (Grey Color)

    AI/ML Overview

    This looks like a 510(k) clearance letter from the FDA for medical gloves, and as such, the concept of "acceptance criteria" and "study that proves the device meets the acceptance criteria" in the context of an AI/ML device isn't directly applicable here.

    This document pertains to a Class I medical device (patient examination gloves), which are largely regulated based on established standards for manufacturing, materials, and basic performance rather than clinical efficacy studies and "acceptance criteria" of an AI algorithm.

    Therefore, many of the specific questions you've asked regarding AI/ML studies (like effect size of AI assistance, sample size for training/test sets, ground truth methodology, and expert qualifications for adjudication) do not apply to this type of device.

    If you are looking for an example of a device with such details, this document is not the right source.

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