BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇲🇾 Malaysia

    PATIENT EXAMINATION GLOVES

    K Number: K904936 · Decision Nov 8, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    151
    Registration Numbers
    151
    Same Product Code
    1953
    Applicant Total
    4
    Review Days
    7

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    Basic Information

    Device Name
    PATIENT EXAMINATION GLOVES
    K Number
    K904936
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Slim River Latex Sdn. Bhd.
    Date Received
    November 1, 1990
    Decision Date
    November 8, 1990
    Product Code
    LYY
    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
    LYY Latex Patient Examination Glove

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    Other Clearances by Slim River Latex Sdn. Bhd.

    K Number Device Name
    K933224 SLIMFLEX - POWDER FREE LATEX EXAMINATION GLOVES
    K926440 POWDER-FREE EXAMINATION GLOVE
    K905033 SLIMFLEX, PATIENT EXAMINATION GLOVES