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

    THAYER MARTIN AGAR & MODIFIED THAYER AGAR

    K Number: K851587 · Decision Apr 30, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    82
    Applicant Total
    28
    Review Days
    14

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    Basic Information

    Device Name
    THAYER MARTIN AGAR & MODIFIED THAYER AGAR
    K Number
    K851587
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.2410
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Preferred Micro-Media
    Date Received
    April 16, 1985
    Decision Date
    April 30, 1985
    Product Code
    JTY
    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
    JTY Culture Media, For Isolation Of Pathogenic Neisseria

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