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510(k) Data Aggregation

    K Number
    K960332
    Device Name
    CARDON PHYSICAL THERAPY TABLE MODEL R28598
    Manufacturer
    CARDON REHABILITATION PRODUCTS, INC.
    Date Cleared
    1996-02-13

    (20 days)

    Product Code
    INQ
    Regulation Number
    890.3760
    Why did this record match?
    Product Code :

    INQ

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K960334
    Device Name
    CARDON PHYSICAL THERAPY TABLE MODEL R27116
    Manufacturer
    CARDON REHABILITATION PRODUCTS, INC.
    Date Cleared
    1996-02-13

    (20 days)

    Product Code
    INQ
    Regulation Number
    890.3760
    Why did this record match?
    Product Code :

    INQ

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K960336
    Device Name
    CARDON PHYSICAL THERAPY TABLE MODEL R27645
    Manufacturer
    CARDON REHABILITATION PRODUCTS, INC.
    Date Cleared
    1996-02-13

    (20 days)

    Product Code
    INQ
    Regulation Number
    890.3760
    Why did this record match?
    Product Code :

    INQ

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K960196
    Device Name
    TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777
    Manufacturer
    TRI W-G, INC.
    Date Cleared
    1996-02-07

    (22 days)

    Product Code
    INQ
    Regulation Number
    890.3760
    Why did this record match?
    Product Code :

    INQ

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question

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