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

    HEMOCHRON MODEL 8000/FACTOR VI PREMIER COAGULATION

    K Number: K930068 · Decision Sep 2, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    39
    Registration Numbers
    39
    Same Product Code
    180
    Applicant Total
    2
    Review Days
    239

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    Basic Information

    Device Name
    HEMOCHRON MODEL 8000/FACTOR VI PREMIER COAGULATION
    K Number
    K930068
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.5425
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Technidyne Corp.
    Date Received
    January 6, 1993
    Decision Date
    September 2, 1993
    Product Code
    JPA
    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
    JPA System, Multipurpose For In Vitro Coagulation Studies

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    Other Clearances by Technidyne Corp.

    K Number Device Name
    K930235 HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY