BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MAMEX

    K Number: K993740 · Decision Nov 26, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    26
    Registration Numbers
    26
    Same Product Code
    175
    Applicant Total
    1
    Review Days
    22

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    Basic Information

    Device Name
    MAMEX
    K Number
    K993740
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.1710
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Medical Systems Group
    Date Received
    November 4, 1999
    Decision Date
    November 26, 1999
    Product Code
    IZH
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IZH System, X-Ray, Mammographic

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