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

    MIO MEDIUM (MOTILITY INDOLE ORNITHINE)

    K Number: K791817 · Decision Oct 1, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29
    Same Product Code
    145
    Applicant Total
    93
    Review Days
    17

    Basic Information

    Device Name
    MIO MEDIUM (MOTILITY INDOLE ORNITHINE)
    K Number
    K791817
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2320
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    ISLE MEDIA AND STERILE PRODUCTS, INC.
    Date Received
    September 14, 1979
    Decision Date
    October 1, 1979
    Product Code
    JSH
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JSH Culture Media, Non-Selective And Differential

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