BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

    018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter

    K Number: K180007 · Decision Apr 19, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    92
    Registration Numbers
    92
    Same Product Code
    402
    Applicant Total
    5
    Review Days
    107

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    Basic Information

    Device Name
    018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter
    K Number
    K180007
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Creagh Medical, Ltd.
    Date Received
    January 2, 2018
    Decision Date
    April 19, 2018
    Product Code
    LIT
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LIT Catheter, Angioplasty, Peripheral, Transluminal

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    Other Clearances by Creagh Medical, Ltd.

    K Number Device Name
    K230191 Arise™ UHP Dilatation Catheter
    K200700 Surmodics Sublime Radial Access 014 RX PTA (Percutaneous Transluminal Angioplasty) Dilatation Catheter
    K113468 ELM PTA BALLON DILATATION CATHETER
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