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

    MULTI-PURPOSE HOLDER

    K Number: K884630 · Decision Nov 22, 1988
    View on FDA
    Classifications
    0
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    80
    Applicant Total
    4
    Review Days
    15

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    Basic Information

    Device Name
    MULTI-PURPOSE HOLDER
    K Number
    K884630
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Med-Dex Intl.
    Date Received
    November 7, 1988
    Decision Date
    November 22, 1988
    Product Code
    LDQ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

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