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

    CELLAVISION DM96 AUTOMATIC HEMATOLOGY ANALYZER

    K Number: K033840 · Decision Feb 10, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    34
    Applicant Total
    7
    Review Days
    62

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    Basic Information

    Device Name
    CELLAVISION DM96 AUTOMATIC HEMATOLOGY ANALYZER
    K Number
    K033840
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.5260
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    CellaVision AB
    Date Received
    December 10, 2003
    Decision Date
    February 10, 2004
    Product Code
    JOY
    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
    JOY Device, Automated Cell-Locating

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