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510(k) Data Aggregation

    K Number
    K992768
    Manufacturer
    Date Cleared
    1999-10-13

    (57 days)

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

    NITRA-TOUCH STERILE POWDER-FREE NITRILE MEDICAL EXAMINATION GLOVE

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

    A disposable device intended for medical purposes that is worn on the examiners hand to prevent contamination between patient and examiner.

    Device Description

    Nitra-Touch™ Sterile examination gloves are disposable device intended for medical purposes that is worn on the examiners hand to prevent contamination between patient and examiner.

    AI/ML Overview

    This document describes the acceptance criteria and the study results for the Nitra-Touch™ Sterile Powder-Free Nitrile Medical Examination Glove by Ansell Perry.

    1. Table of Acceptance Criteria and Reported Device Performance

    CharacteristicsAcceptance Criteria (Standard)Reported Device Performance
    DimensionsMeets ASTM D 6319Meets ASTM D 6319
    Physical Properties:
    Tensile Strength, minimumMeets ASTM D 6319 (14 MPa)Exceeds ASTM D 6319 (14 MPa)
    Freedom from holesMeets ASTM D 6319, Meets ASTM D 5151Meets ASTM D 6319, Meets ASTM D 5151
    Powder-FreeNot more than 2 mg residue by mass, Meets ASTM D 6124Not more than 2 mg residue by mass, Meets ASTM D 6124
    Biocompatibility
    Primary Skin Irritation (Rabbits)Acceptable (Passes)Passes
    Guinea Pig SensitizationAcceptable (Passes)Passes

    2. Sample size used for the test set and the data provenance

    The document does not specify the exact sample sizes used for each individual test (e.g., for dimensions, tensile strength, freedom from holes, powder-free, or biocompatibility). However, it indicates that the tests were conducted according to established ASTM standards (D 6319, D 5151, D 6124). These standards often prescribe minimum sample sizes for testing.

    The data provenance is not explicitly stated as "country of origin" or "retrospective/prospective." However, the tests are "non-clinical tests" conducted to demonstrate conformity with recognized standards like ASTM, which are generally performed in a controlled laboratory setting.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

    This information is not applicable and not provided in the document. The "ground truth" for medical examination gloves is established by objective, quantifiable measurements against defined performance standards (ASTM standards) and biocompatibility tests, rather than expert consensus on subjective interpretations.

    4. Adjudication method for the test set

    This information is not applicable. The performance is measured against objective standards, not through subjective adjudication.

    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

    This information is not applicable. This device is a medical examination glove, not an AI-powered diagnostic or assistive tool. Therefore, MRMC studies and AI-related effect sizes are irrelevant.

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

    This information is not applicable. This is a physical medical device, not an algorithm.

    7. The type of ground truth used

    The ground truth used for evaluating the Nitra-Touch™ gloves is defined by:

    • Established Industry Standards: ASTM Standard D 6319 (Nitrile Examination Gloves for Medical Application), ASTM D 5151 (Freedom from Holes), and ASTM D 6124 (Powder Residue).
    • Biocompatibility Test Pass/Fail Criteria: Standard methods for assessing Primary Skin Irritation and Guinea Pig Sensitization.
    • FDA Hole Requirements: The gloves also meet FDA hole requirements.

    These ground truths are objective and quantitatively measurable.

    8. The sample size for the training set

    This information is not applicable. There is no concept of a "training set" for a physical medical device like an examination glove. These products are manufactured and then tested for compliance with specifications.

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

    This information is not applicable, as there is no training set for this type of device.

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