BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    DESERET MULTILUMEN SUBCLAVIAN CATHETER

    K Number: K895735 · Decision May 18, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    151
    Registration Numbers
    151
    Same Product Code
    1953
    Applicant Total
    20
    Review Days
    233

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    Basic Information

    Device Name
    DESERET MULTILUMEN SUBCLAVIAN CATHETER
    K Number
    K895735
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Deseret Medical, Inc.
    Date Received
    September 27, 1989
    Decision Date
    May 18, 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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