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

    LOMBARD DOWELL AGAR BASE

    K Number: K864014 · Decision Oct 29, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    17
    Registration Numbers
    17
    Same Product Code
    50
    Applicant Total
    67
    Review Days
    14

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    Basic Information

    Device Name
    LOMBARD DOWELL AGAR BASE
    K Number
    K864014
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2330
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Gibco Laboratories Life Technologies, Inc.
    Date Received
    October 15, 1986
    Decision Date
    October 29, 1986
    Product Code
    KZI
    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
    KZI Culture Media, Enriched

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