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

    SYSMEX E-5000 FULLY AUTOMATED HEMATOLOGY SYSTEM

    K Number: K855116 · Decision Feb 24, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    379
    Applicant Total
    33
    Review Days
    63

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    Basic Information

    Device Name
    SYSMEX E-5000 FULLY AUTOMATED HEMATOLOGY SYSTEM
    K Number
    K855116
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.5220
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Applicant
    Toa Medical Electronics USA, Inc.
    Date Received
    December 23, 1985
    Decision Date
    February 24, 1986
    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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