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

    LIGHT-PEN SYSTEM FOR QUANTI. ANALY.

    K Number: K772158 · Decision Nov 22, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    63
    Registration Numbers
    63
    Same Product Code
    176
    Applicant Total
    86
    Review Days
    6

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    Basic Information

    Device Name
    LIGHT-PEN SYSTEM FOR QUANTI. ANALY.
    K Number
    K772158
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1435
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Varian Assoc., Inc.
    Date Received
    November 16, 1977
    Decision Date
    November 22, 1977
    Product Code
    DXG
    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
    DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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