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

    QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)

    K Number: K960827 · Decision May 17, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    379
    Applicant Total
    13
    Review Days
    78

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    Basic Information

    Device Name
    QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)
    K Number
    K960827
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.5220
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Becton Dickinson Diagnostic Instrument Systems
    Date Received
    February 29, 1996
    Decision Date
    May 17, 1996
    Product Code
    GKZ
    Advisory Committee
    Hematology
    Review Advisory Committee
    HE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GKZ Counter, Differential Cell

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