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

    NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET) with Preloaded Stylet

    K Number: K172208 · Decision Feb 16, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    132
    Registration Numbers
    132
    Same Product Code
    240
    Applicant Total
    1
    Review Days
    207

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    Basic Information

    Device Name
    NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET) with Preloaded Stylet
    K Number
    K172208
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5730
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Nevap, Inc.
    Date Received
    July 24, 2017
    Decision Date
    February 16, 2018
    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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