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

    ENDO-MED TUBE FOR ENDOTRACHEAL MED

    K Number: K810059 · Decision Feb 26, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    9
    Applicant Total
    42
    Review Days
    44

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    Basic Information

    Device Name
    ENDO-MED TUBE FOR ENDOTRACHEAL MED
    K Number
    K810059
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5170
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Ackrad Laboratories
    Date Received
    January 13, 1981
    Decision Date
    February 26, 1981
    Product Code
    CCT
    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
    CCT Applicator (Laryngo-Tracheal), Topical Anesthesia

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