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

    LUX-Dx II (M302); LUX-Dx II+ (M312)

    K Number: K231328 · Decision Aug 19, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    32
    Applicant Total
    432
    Review Days
    103

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    Basic Information

    Device Name
    LUX-Dx II (M302); LUX-Dx II+ (M312)
    K Number
    K231328
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1025
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Boston Scientific Corp
    Date Received
    May 8, 2023
    Decision Date
    August 19, 2023
    Product Code
    MXD
    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
    MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)

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