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

    NCONTACT COAGULATION SYSTEM KIT

    K Number: K062539 · Decision Dec 1, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    7
    Review Days
    94

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    Basic Information

    Device Name
    NCONTACT COAGULATION SYSTEM KIT
    K Number
    K062539
    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
    Ncontact Surgical, Inc.
    Date Received
    August 29, 2006
    Decision Date
    December 1, 2006
    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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    Other Clearances by Ncontact Surgical, Inc.

    K Number Device Name
    K142084 EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX
    K120857 EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX
    K090202 NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125
    K082203 NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025
    K071819 NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515
    K063012 NCONTACT COAGULATION SYSTEM KIT, MODEL CSK