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510(k) Data Aggregation

    K Number
    K031754
    Date Cleared
    2003-06-30

    (91 days)

    Product Code
    Regulation Number
    880.6250
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Powder Free Latex Examination Gloves, Non-Sterile (Contains 50 micrograms or less of Water Extractable Protein per gram) is a disposable device and made of Natural Rubber Latex intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.

    Device Description

    The Powder Free Latex Examination Gloves, Non Sterile (Contains 50 micrograms or less of Total Water Extractable Protein per gram) meets all the requirements of ASTM standard D 3578 - 01a 22 and FDA 1000 ml Water Leak Test.

    AI/ML Overview

    Here's an analysis of the provided text regarding the acceptance criteria and study for the PT. Mandiri Inti Buana examination gloves:

    Overview:

    This submission describes a Class I medical device (Powder Free Latex Examination Gloves, Non-Sterile) and seeks a 510(k) clearance based on substantial equivalence to legally marketed predicate devices. The "study" here refers to non-clinical performance testing conducted to demonstrate compliance with established standards.

    1. Table of Acceptance Criteria and Reported Device Performance

    CHARACTERISTICSACCEPTANCE CRITERIA (STANDARDS)REPORTED DEVICE PERFORMANCE
    DimensionsD 3578 - 01ae2Meets
    Physical PropertiesD 3578 - 01ae2Meets
    Freedom from PinholesD 3578 - 01ae2, FDA 21 CFR 800.20 (FDA 1000 ml Water Leak Test)Meets
    Powder ResidueD 3578 - 01ae2, D 6124 - 01
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