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

    TABLE, TREATMENT, THERAPY, PHYSICAL

    K Number: K770723 · Decision Jul 11, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    9
    Registration Numbers
    9
    Same Product Code
    3
    Applicant Total
    2
    Review Days
    83

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    Basic Information

    Device Name
    TABLE, TREATMENT, THERAPY, PHYSICAL
    K Number
    K770723
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3520
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Chattanooga Pharmacal Co.
    Date Received
    April 19, 1977
    Decision Date
    July 11, 1977
    Product Code
    INT
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    INT Plinth

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    Other Clearances by Chattanooga Pharmacal Co.

    K Number Device Name
    K770724 TRACTION DEVICES, INTERMITTENT, TX