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

    NEUROSEARCH-24 OR NRS-24

    K Number: K904269 · Decision Jun 4, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    96
    Registration Numbers
    96
    Same Product Code
    188
    Applicant Total
    3
    Review Days
    259

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    Basic Information

    Device Name
    NEUROSEARCH-24 OR NRS-24
    K Number
    K904269
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1400
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Lexicor Medical Technology, Inc.
    Date Received
    September 18, 1990
    Decision Date
    June 4, 1991
    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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    Other Clearances by Lexicor Medical Technology, Inc.

    K Number Device Name
    K961645 MRS-2D
    K915820 NEUROSEARCH-24 OR NRS-24