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

    Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set

    K Number: K232524 · Decision Oct 18, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    57
    Registration Numbers
    57
    Same Product Code
    96
    Applicant Total
    7
    Review Days
    61

    Basic Information

    Device Name
    Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
    K Number
    K232524
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Perfuze Ltd.
    Date Received
    August 18, 2023
    Decision Date
    October 18, 2023
    Product Code
    NRY
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    NRY Catheter, Thrombus Retriever

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