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

    SYSMEX CC-170

    K Number: K830507 · Decision May 13, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21
    Same Product Code
    129
    Applicant Total
    33
    Review Days
    85

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    Basic Information

    Device Name
    SYSMEX CC-170
    K Number
    K830507
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.5200
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Applicant
    Toa Medical Electronics USA, Inc.
    Date Received
    February 17, 1983
    Decision Date
    May 13, 1983
    Product Code
    GKL
    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
    GKL Counter, Cell, Automated (Particle Counter)

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    Other Clearances by Toa Medical Electronics USA, Inc.

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    K912494 SYSMEX(TM) R-3000 AUTOMATED RETICULOCYTE ANALYZER
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