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

    SURGICAL HAMMERS

    K Number: K802524 · Decision Nov 12, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    271
    Registration Numbers
    271
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    27

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    Basic Information

    Device Name
    SURGICAL HAMMERS
    K Number
    K802524
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Midshore Welding Corp.
    Date Received
    October 16, 1980
    Decision Date
    November 12, 1980
    Product Code
    FZY
    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
    FZY Hammer, Surgical