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

    MODEL 503FB

    K Number: K842759 · Decision Jan 18, 1985
    View on FDA
    Classifications
    0
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    82
    Applicant Total
    2
    Review Days
    186

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    Basic Information

    Device Name
    MODEL 503FB
    K Number
    K842759
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Atrix
    Date Received
    July 16, 1984
    Decision Date
    January 18, 1985
    Product Code
    LOS
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

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