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

    SPECIMEX DC

    K Number: K900740 · Decision May 11, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    64
    Registration Numbers
    64
    Same Product Code
    52
    Applicant Total
    1
    Review Days
    84

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    Basic Information

    Device Name
    SPECIMEX DC
    K Number
    K900740
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1350
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Soredex Medical Systems
    Date Received
    February 16, 1990
    Decision Date
    May 11, 1990
    Product Code
    GXZ
    Advisory Committee
    Neurology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GXZ Electrode, Needle

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