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

    OPUS FERRITIN TEST SYSTEM

    K Number: K915838 · Decision Mar 18, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1
    Same Product Code
    1
    Applicant Total
    35
    Review Days
    85

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    Basic Information

    Device Name
    OPUS FERRITIN TEST SYSTEM
    K Number
    K915838
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.5510
    Medical Specialty
    Immunology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Pb Diagnostic Systems, Inc.
    Date Received
    December 24, 1991
    Decision Date
    March 18, 1992
    Product Code
    DGE
    Advisory Committee
    Immunology
    Review Advisory Committee
    IM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DGE Igd, Rhodamine, Antigen, Antiserum, Control

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