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

    URESIL THORACIC VENT

    K Number: K863561 · Decision Sep 23, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    276
    Same Product Code
    47
    Applicant Total
    45
    Review Days
    11

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    Basic Information

    Device Name
    URESIL THORACIC VENT
    K Number
    K863561
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Uresil Corp.
    Date Received
    September 12, 1986
    Decision Date
    September 23, 1986
    Product Code
    KDQ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KDQ Bottle, Collection, Vacuum

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