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510(k) Data Aggregation

    K Number
    K093300
    Date Cleared
    2009-10-30

    (9 days)

    Product Code
    Regulation Number
    878.4460
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ESTEEM SMT POLYISOPRENE POWDER-FREE SURGICAL STERILE GLOVES

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

    These powder-free surgeon's gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination in the environments within hospitals and other healthcare facilities.

    Device Description

    Esteem SMT Polyisoprene Powder-Free Surgical gloves are formulated using synthetic rubber latex. They are offered powder-free and sterile.

    AI/ML Overview

    The Esteem SMT Polyisoprene Powder-Free Surgical Gloves were subject to several performance tests to demonstrate substantial equivalence. The acceptance criteria and reported device performance are summarized below:

    1. Table of Acceptance Criteria and Reported Device Performance

    Test:Acceptance Criteria:Reported Device Performance:
    Primary Skin IrritationGloves must be non-irritating.Gloves are non-irritating.
    Guinea Pig MaximizationGloves must not display any potential for sensitization.Gloves do not display any potential for sensitization.
    DimensionsMust meet requirements of ASTM D3577.Gloves meet requirements of ASTM D3577.
    Physical CharacteristicsMust meet requirements for rubber surgical gloves per ASTM D3577.Gloves meet requirements for rubber surgical gloves per ASTM D3577.
    Freedom from HolesMust meet requirements of 21 CFR 800.20 and ASTM D3577.Gloves meet requirements of 21 CFR 800.20 and ASTM D3577.
    Powder ResidualMust meet powder level requirements for "Powder-Free" designation per ASTM D3577, tested using ASTM standard D6124.Results generated values below 2mg of residual powder per glove, meeting the "Powder-Free" designation.

    2. Sample size used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective)

    The document does not specify the exact sample sizes used for each test. The tests were performed by Cardinal Healthcare 222 LTD. in Rayong, Thailand, which is the country of origin. The study appears to be prospective testing of the manufactured gloves.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience)

    This product is a medical glove, not an AI or imaging device that requires interpretation by medical experts. Therefore, the concept of "experts establishing ground truth for the test set" and their qualifications as typically understood in AI/imaging studies (e.g., radiologists) is not applicable. The ground truth for glove performance is established by standardized material and physiological testing methods.

    4. Adjudication method (e.g. 2+1, 3+1, none) for the test set

    Not applicable as this is not an AI or imaging device requiring human adjudication of results from a diagnostic test. Performance is determined by established physical and biological testing standards.

    5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

    Not applicable as this is a physical medical device (surgical gloves), not an AI-assisted diagnostic tool.

    6. If a standalone (i.e. algorithm only without human-in-the loop performance) was done

    Not applicable as this is a physical medical device. The "standalone" performance here refers to the glove's intrinsic properties as measured by the specified tests, without human intervention in the measurement of those properties (although humans would be performing the tests).

    7. The type of ground truth used (expert consensus, pathology, outcomes data, etc)

    The ground truth for this device is based on established industry standards and regulatory requirements for medical gloves. This includes:

    • ASTM D3577: Standard Specification for Rubber Surgical Gloves.
    • 21 CFR 800.20: Regulations regarding freedom from holes in surgeon's gloves.
    • ASTM D6124: Standard Test Method for Residual Powder on Medical Gloves.
    • Biological safety standards: For skin irritation and sensitization (e.g., Primary Skin Irritation and Guinea Pig Maximization tests).

    These standards define the objective criteria and methods against which the glove's performance is measured.

    8. The sample size for the training set

    Not applicable. This is a physical device, not a machine learning model, hence no "training set" in the context of AI.

    9. How the ground truth for the training set was established

    Not applicable for a physical device.

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