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

    VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR

    K Number: K051644 · Decision Aug 11, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    10
    Review Days
    52

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    Basic Information

    Device Name
    VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR
    K Number
    K051644
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Valleylab
    Date Received
    June 20, 2005
    Decision Date
    August 11, 2005
    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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    K043273 LIGASURE VESSEL SEALING SYSTEM. LIGASURE INSTRUMENTS
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    K041587 LIGASURE PRECISE MODEL #LS1200/LIGASURE 5MM LAPAROSCOPIC SEALER DIVIDER MODEL # LS1500