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

    LifeWatch Mobile Cardiac Telemetry 3 Lead LifeWatch MCT 3L

    K Number: K170565 · Decision Aug 1, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    20
    Applicant Total
    1
    Review Days
    155

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    Basic Information

    Device Name
    LifeWatch Mobile Cardiac Telemetry 3 Lead LifeWatch MCT 3L
    K Number
    K170565
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1025
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Lifewatch Services, Inc.
    Date Received
    February 27, 2017
    Decision Date
    August 1, 2017
    Product Code
    QYX
    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
    QYX Outpatient Cardiac Telemetry

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