BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Wearable Automated External Defibrillator

    PMA: P010030 · Supplement: S062 · Decision Jun 30, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8

    Basic Information

    Device Name
    Wearable Automated External Defibrillator
    Trade Name
    LIFEVEST WEARABLE DEFIBRILLATOR
    PMA Number
    P010030
    Supplement Number
    S062
    Device Class
    FDA Class 3
    Product Code
    MVK
    Generic Name
    Wearable automated external defibrillator
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    June 30, 2015
    Date Received
    June 4, 2015
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    MAKE THE ¿MONITOR DETECT AND TREAT¿ TEST PERMANENT; AUTOMATE THE MONITOR DETECT AND TREAT TEST; REPLACE THE EXISTING AUTOTEST MONITOR PULSE TEST WITH THE AUTOMATED MONITOR DETECT AND TREAT TEST IN A SUBSEQUENT STEP OF THE PRODUCTION PROCESS.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MVK Wearable Automated External Defibrillator