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

    L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION

    K Number: K853099 · Decision Dec 3, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    143
    Registration Numbers
    144
    Same Product Code
    136
    Applicant Total
    5
    Review Days
    133

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    Basic Information

    Device Name
    L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATION
    K Number
    K853099
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4290
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    L.O.N. Research, Inc.
    Date Received
    July 23, 1985
    Decision Date
    December 3, 1985
    Product Code
    DTL
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

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