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

    MULTIWELL CULTURE PLATE INSERTS

    K Number: K890542 · Decision Feb 14, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    7
    Applicant Total
    632
    Review Days
    11

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    Basic Information

    Device Name
    MULTIWELL CULTURE PLATE INSERTS
    K Number
    K890542
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    864.2240
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Applicant
    Bd Becton Dickinson Vacutainer Systems Preanalytic
    Date Received
    February 3, 1989
    Decision Date
    February 14, 1989
    Product Code
    KIZ
    Advisory Committee
    Hematology
    Review Advisory Committee
    PA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KIZ Dish, Tissue Culture

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