BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇭🇰 Hong Kong

    LAPASCOPIC INSTRUMENTS AND ELECTRODE TIPS

    K Number: K030831 · Decision Jun 15, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    14
    Review Days
    459

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    Basic Information

    Device Name
    LAPASCOPIC INSTRUMENTS AND ELECTRODE TIPS
    K Number
    K030831
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Modern Medical Equipment Mfg., Ltd.
    Date Received
    March 14, 2003
    Decision Date
    June 15, 2004
    Product Code
    GEI
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GEI Electrosurgical, Cutting & Coagulation & Accessories

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    K043036 NON-STICK ELECTRODE
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