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

    VASCUTRAK II PTA DILATATION CATHETER

    K Number: K073025 · Decision Nov 9, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    32
    Registration Numbers
    32
    Same Product Code
    44
    Applicant Total
    1
    Review Days
    14

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    Basic Information

    Device Name
    VASCUTRAK II PTA DILATATION CATHETER
    K Number
    K073025
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Thermopeutix, Inc. Dba Ymed, Inc.
    Date Received
    October 26, 2007
    Decision Date
    November 9, 2007
    Product Code
    PNO
    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
    PNO Catheter, Percutaneous, Cutting/Scoring

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