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

    CARDON PHYSICAL THERAPY TABLE MODEL R28598

    K Number: K960332 · Decision Feb 13, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    101
    Applicant Total
    16
    Review Days
    20

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    Basic Information

    Device Name
    CARDON PHYSICAL THERAPY TABLE MODEL R28598
    K Number
    K960332
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3760
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Cardon Rehabilitation Products, Inc.
    Date Received
    January 24, 1996
    Decision Date
    February 13, 1996
    Product Code
    INQ
    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
    INQ Table, Powered

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    Other Clearances by Cardon Rehabilitation Products, Inc.

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    K950873 CARDON PHYSICAL THERAPY TABLES MODELS: R27622
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