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

    S & W SW52E W/POWER BACK LIFT

    K Number: K832768 · Decision Sep 20, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    44
    Registration Numbers
    44
    Same Product Code
    13
    Applicant Total
    6
    Review Days
    35

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    Basic Information

    Device Name
    S & W SW52E W/POWER BACK LIFT
    K Number
    K832768
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4960
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    S & W Enterprises, Inc.
    Date Received
    August 16, 1983
    Decision Date
    September 20, 1983
    Product Code
    LGX
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LGX Table, Examination, Medical, Powered

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