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

    DIACROM * HEPARIN

    K Number: K832373 · Decision Sep 29, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    45
    Applicant Total
    28
    Review Days
    73

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    Basic Information

    Device Name
    DIACROM * HEPARIN
    K Number
    K832373
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.7525
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Applicant
    Wellcome Diagnostics
    Date Received
    July 18, 1983
    Decision Date
    September 29, 1983
    Product Code
    KFF
    Advisory Committee
    Hematology
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    KFF Assay, Heparin

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