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

    POWER EXAMINATION TABLE

    K Number: K882010 · Decision Jul 13, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    44
    Registration Numbers
    44
    Same Product Code
    13
    Applicant Total
    1
    Review Days
    61

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    Basic Information

    Device Name
    POWER EXAMINATION TABLE
    K Number
    K882010
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4960
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Enochs Mfg., Inc.
    Date Received
    May 13, 1988
    Decision Date
    July 13, 1988
    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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