BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    HP PTA Balloon Dilatation Catheter

    K Number: K231402 · Decision Dec 20, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    92
    Registration Numbers
    92
    Same Product Code
    402
    Applicant Total
    5
    Review Days
    219

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    Basic Information

    Device Name
    HP PTA Balloon Dilatation Catheter
    K Number
    K231402
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Kossel Medtech (Suzhou) Co., Ltd.
    Date Received
    May 15, 2023
    Decision Date
    December 20, 2023
    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 Kossel Medtech (Suzhou) Co., Ltd.

    K Number Device Name
    K221245 PTA Balloon Dilatation Catheter
    K211349 Selebrek PTCA Balloon Dilatation Catheter
    K211393 Selethru(TM) NC PTCA Balloon Dilatation Catheter
    K182699 Selethru PTCA Balloon Dilatation Catheter