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

    Q.P. PREAMPLIFIER SYS

    K Number: K841683 · Decision Jun 7, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    96
    Registration Numbers
    96
    Same Product Code
    188
    Applicant Total
    6
    Review Days
    45

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    Basic Information

    Device Name
    Q.P. PREAMPLIFIER SYS
    K Number
    K841683
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1400
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Bio-Scan, Inc.
    Date Received
    April 23, 1984
    Decision Date
    June 7, 1984
    Product Code
    GWQ
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GWQ Full-Montage Standard Electroencephalograph

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