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510(k) Data Aggregation

    K Number
    K050071
    Date Cleared
    2005-05-11

    (119 days)

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

    MEDISPO (POWDERED) AND MEDISPO-PF (POWDER-FREE) SURGEONS GLOVE

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

    MEDISPO powdered surgeon's gloves are sterile disposable devices made of natural rubber latex that bears powder to facilitate donning, and it is intended to be worn on the hands, usually in surgical settings, to provide a barrier against potentially infectious materials and other contaminants.

    MEDISPO-PF powder-free surgeon's gloves are sterile disposable devices made of natural rubber latex (that may bear a trace amount of glove powder) and is intended to he worn on the hands, usually in surgical settings, to provide a barrier against potentially infectious materials and other contaminants.

    Device Description

    MEDISPO and MEDISPO-PF meet the requirements for surgical gloves described by ASTM D3577.

    AI/ML Overview

    Acceptance Criteria and Device Performance Study for H.B.M. USA Co., Inc. – Latex Sterile Surgical Gloves

    1. Table of Acceptance Criteria and Reported Device Performance

    Acceptance CriteriaReported Device Performance
    Physical Properties
    Meets requirements for surgical gloves described by ASTM D3577Tests conducted per ASTM D3577 indicate the product meets the requirements.
    Biocompatibility
    No sensitizationTests indicate no sensitization.
    No irritationTests indicate no irritation.

    2. Sample Size Used for the Test Set and Data Provenance

    The document does not explicitly state the sample size used for the test set or the data provenance (e.g., country of origin, retrospective/prospective). It only mentions "Tests conducted per ASTM D3577." ASTM D3577 itself outlines standard test methods and specifications for rubber surgical gloves, which would implicitly define sample sizes for specific tests (e.g., tensile strength, elongation, barrier integrity).

    3. Number of Experts Used to Establish Ground Truth and Qualifications

    Not applicable. For medical devices like surgical gloves, "ground truth" is typically established through adherence to recognized international standards (like ASTM D3577), which specify objective laboratory testing methods rather than requiring expert consensus on subjective observations.

    4. Adjudication Method for the Test Set

    Not applicable. The evaluation of surgical gloves against ASTM D3577 involves objective laboratory measurements and tests, not subjective interpretations requiring an adjudication method.

    5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

    Not applicable. This type of study is relevant for diagnostic imaging or screening devices where human readers interpret complex data. Surgical gloves are evaluated based on their physical and biocompatibility properties, not on reader performance.

    6. Standalone (Algorithm Only) Performance

    Not applicable. Surgical gloves are not an AI-driven device or an algorithm. Their performance is assessed through physical and chemical testing.

    7. Type of Ground Truth Used

    The "ground truth" for the device's performance is established by adherence to the specifications and test methods outlined in the ASTM D3577 standard. This includes objective measurements of properties like dimensions, physical integrity (e.g., absence of holes), tensile strength, and elongation, as well as biocompatibility tests for irritation and sensitization.

    8. Sample Size for the Training Set

    Not applicable. This device is not an AI/machine learning model, so there is no concept of a "training set."

    9. How the Ground Truth for the Training Set was Established

    Not applicable. As there is no training set, this question is not relevant.

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