LogoFDA 510(k) Search
Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K024215
    Device Name
    ENERTRON CPR JACK
    Manufacturer
    ENERTRON ENGINEERING CO.
    Date Cleared
    2004-05-14

    (511 days)

    Product Code
    DRM
    Regulation Number
    870.5200
    Why did this record match?
    Applicant Name (Manufacturer) :

    ENERTRON ENGINEERING CO.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The device is an external device that is manually powered and is used to compress the chest periodically in the region of the heart to provide blood flow during cardiac arrest for adult patients.
    Device Description
    The ENERTRON CPR JACK is a portable cardiopulmonary resuscitation device with a patented feature of consistent and precision compression depth. It includes a frame structure and a compression mechanism. The compression mechanism has a handle connected with a connecting bar to drive a plunger. The compression mechanism keeps the plunging movements in a perpendicular direction. A depth controlling scale is included on the frame structure for presetting the compression depth of the plunger.
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1