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

    UMBRELLA KEEL

    K Number: K841348 · Decision May 2, 1984
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    6
    Review Days
    30

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    Basic Information

    Device Name
    UMBRELLA KEEL
    K Number
    K841348
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    E. Benson Hood Laboratories, Inc.
    Date Received
    April 2, 1984
    Decision Date
    May 2, 1984
    Advisory Committee
    Unknown
    Review Advisory Committee
    GU
    Third Party
    N

    Other Clearances by E. Benson Hood Laboratories, Inc.

    K Number Device Name
    K983878 CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE
    K841350 SALIVARY BYPASS TUBE
    K841349 ESOPHAGEAL TUBE
    K841266 MONTGOMERY TRACHEAL T-TUBE
    K841347 LARYNGEAL STENT