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

    CG+ ARROW PICC POWERED BY ARROW VPS STYLET

    K Number: K123759 · Decision Jan 3, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    90
    Registration Numbers
    90
    Same Product Code
    301
    Applicant Total
    2
    Review Days
    27

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    Basic Information

    Device Name
    CG+ ARROW PICC POWERED BY ARROW VPS STYLET
    K Number
    K123759
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    880.5970
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Arrow International, Inc. (Subsidiary of Teleflex
    Date Received
    December 7, 2012
    Decision Date
    January 3, 2013
    Product Code
    LJS
    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
    LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

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    Other Clearances by Arrow International, Inc. (Subsidiary of Teleflex

    K Number Device Name
    K161765 CG+ Arrow JACC