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    FDA 510(k) FDA class 1 Substantially Equivalent 🇹🇭 Thailand

    OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED, BLUE

    K Number: K983725 · Decision Dec 7, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    380
    Registration Numbers
    380
    Same Product Code
    1171
    Applicant Total
    8
    Review Days
    46

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    Basic Information

    Device Name
    OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED, BLUE
    K Number
    K983725
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Omnigrace , Ltd.
    Date Received
    October 22, 1998
    Decision Date
    December 7, 1998
    Product Code
    LZA
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LZA Polymer Patient Examination Glove

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    Other Clearances by Omnigrace , Ltd.

    K Number Device Name
    K994246 OMNI GRACE NITRILE, BLUE, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED
    K993419 OMNIGRACE LATEX EXAMINATION GLOVE, POWDER-FREE; POLYMER COATED WITH PROTEIN CLAIM (50 MICROGRAMS OR LESS)
    K993050 OMNI GRACE NITRILE, GREEN, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED
    K991846 PATIENT EXAMINATION GLOVE, NITRILE, POWDERED, TURQUOISE, NON-STERILE
    K991845 PATIENT EXAMINATION GLOVES, NITRILE POWDER FREE, TURQUOISE,NON-STERILE.
    K983730 OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE, BLUE
    K973134 OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED