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

    NICOLET ELECTROCAUTERY DETECTOR

    K Number: K020955 · Decision Apr 17, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    140
    Registration Numbers
    140
    Same Product Code
    96
    Applicant Total
    10
    Review Days
    23

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    Basic Information

    Device Name
    NICOLET ELECTROCAUTERY DETECTOR
    K Number
    K020955
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    874.1820
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Nicolet Biomedical, Inc.
    Date Received
    March 25, 2002
    Decision Date
    April 17, 2002
    Product Code
    ETN
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    ETN Stimulator, Nerve

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