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

    U.S. DIAGNOSTIC INC. HEMOGLOBIN TEST (DRY PACK)

    K Number: K862641 · Decision Aug 21, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    9
    Registration Numbers
    9
    Same Product Code
    38
    Applicant Total
    22
    Review Days
    41

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    Basic Information

    Device Name
    U.S. DIAGNOSTIC INC. HEMOGLOBIN TEST (DRY PACK)
    K Number
    K862641
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    864.7500
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Applicant
    U. S. Diagnostics, Inc.
    Date Received
    July 11, 1986
    Decision Date
    August 21, 1986
    Product Code
    KHG
    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
    KHG Whole Blood Hemoglobin Determination

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