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

    MEDONIC CA620/530 HEMATOLOGY ANALYZER

    K Number: K032214 · Decision Jan 29, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    379
    Applicant Total
    2
    Review Days
    192

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    Basic Information

    Device Name
    MEDONIC CA620/530 HEMATOLOGY ANALYZER
    K Number
    K032214
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.5220
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Boule Medical AB
    Date Received
    July 21, 2003
    Decision Date
    January 29, 2004
    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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