BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    HEMATOXYLIN

    K Number: K811802 · Decision Jul 28, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    40
    Registration Numbers
    40
    Same Product Code
    13
    Applicant Total
    33
    Review Days
    34

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    Basic Information

    Device Name
    HEMATOXYLIN
    K Number
    K811802
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    864.1850
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Applicant
    Richard-Allan Medical Ind., Inc.
    Date Received
    June 24, 1981
    Decision Date
    July 28, 1981
    Product Code
    HYJ
    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
    HYJ Hematoxylin

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