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

    ARROW PNEUMOTHORAX KIT, AK-01500

    K Number: K883905 · Decision Jan 19, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    331
    Registration Numbers
    331
    Same Product Code
    83
    Applicant Total
    110
    Review Days
    126

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    Basic Information

    Device Name
    ARROW PNEUMOTHORAX KIT, AK-01500
    K Number
    K883905
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Applicant
    Arrow Intl., Inc.
    Date Received
    September 15, 1988
    Decision Date
    January 19, 1989
    Product Code
    JOL
    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
    JOL Catheter And Tip, Suction

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