BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    THOREK SCISSORS 7 1/4 & 10

    K Number: K771806 · Decision Oct 4, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    257
    Registration Numbers
    257
    Same Product Code
    51
    Applicant Total
    18
    Review Days
    11

    Basic Information

    Device Name
    THOREK SCISSORS 7 1/4 & 10
    K Number
    K771806
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    J. SKLAR MFG. CO., INC.
    Date Received
    September 23, 1977
    Decision Date
    October 4, 1977
    Product Code
    FZT
    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
    FZT Cutter, Surgical

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