BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇷🇺 Russian Federation

    Mitsar-EEG

    K Number: K143233 · Decision Aug 13, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    96
    Registration Numbers
    96
    Same Product Code
    188
    Applicant Total
    1
    Review Days
    276

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    Mitsar-EEG
    K Number
    K143233
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1400
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Mitsar Co., Ltd.
    Date Received
    November 10, 2014
    Decision Date
    August 13, 2015
    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

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (GWQ), ordered by most recent decision date.

    Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)

    FDA 510(k)
    FDA Class 2 ·Neurology

    New Wave System

    FDA 510(k)
    FDA Class 2 ·Neurology

    Flexset System

    FDA 510(k)
    FDA Class 2 ·Neurology

    Neuronaute Plus

    FDA 510(k)
    FDA Class 2 ·Neurology

    Q21

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPARK Scan

    FDA 510(k)
    FDA Class 2 ·Neurology
    View all