BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    KENDALL CURITY ENDOTRACHEAL TUBES

    K Number: K892432 · Decision Jun 12, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    132
    Registration Numbers
    132
    Same Product Code
    240
    Applicant Total
    63
    Review Days
    63

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    Basic Information

    Device Name
    KENDALL CURITY ENDOTRACHEAL TUBES
    K Number
    K892432
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5730
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    The Kendal Co.
    Date Received
    April 10, 1989
    Decision Date
    June 12, 1989
    Product Code
    BTR
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BTR Tube, Tracheal (W/Wo Connector)

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    K942664 KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
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    K892438 KENDALL CURITY INTRAVASCULAR CUT DOWN TUBES
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