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    • FDA grants clearance...

    FDA grants clearance to new Blood Flow Monitoring Device for peripheral artery disease

    Written by Dr. Kamal Kant Kohli Kohli Published On 2019-10-03T19:28:40+05:30  |  Updated On 3 Oct 2019 7:28 PM IST
    FDA grants clearance to new Blood Flow Monitoring Device for peripheral artery disease

    A new blood flow monitoring device, FlowMet-R, has received clearance from the Food and Drug Administration (FDA). This clearance allows Laser Associated Sciences (LAS), a medical device company based in Irvine to market and sell the FlowMet-R.


    according to the American Heart Association,peripheral artery disease affects over 200 million people worldwide, often goes undiagnosed and when left untreated, can result in amputation.The non-invasive portable device addresses a critical unmet need for vascular specialists who are seeking improved methods to detect and measure treatment efficacy for peripheral artery disease (PAD).


    The FlowMet-R is simple for clinicians to use as the device is compact and clips directly onto a patient's toe. The technology includes a small laser diode and a camera the size of a postage stamp to measure blood flow in the digit in real-time. This measurement reflects the severity of vascular disease upstream of the digit. Vascular clinicians who use FlowMet-R believe it fills an essential need via intraprocedural monitoring, enabling them to make better decisions about their treatment during surgery.


    "By directly measuring limb perfusion during surgeries, physicians can see for the first time whether peripheral blood flow in being improved in real-time. This reduces the ambiguity that clinicians currently face in knowing not only if an intervention is effective, but how effective it is. It is inspiring for us to receive such positive feedback from both the medical community and receive clearance from the FDA so quickly," says Sean White, CEO of LAS.


    The company also recently completed a clinical study in which FlowMet-R measurements demonstrated improved accuracy in detecting advanced vascular disease compared to standard vascular assessments. "The results were very impactful toward improving patient care, and we look forward to publishing the results shortly," adds White.


    LAS continues to collaborate with clinicians to develop new technologies that will improve outcomes for patients. The company is also exploring opportunities to build products for home use as well.

    American Heart Associationblood flowcaliforniaFDAFlowMet-RFood and Drug AdministrationLaser Associated Sciencesmedical deviceperipheral artery diseaseSean Whitevia intraprocedural monitoring

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    Dr. Kamal Kant Kohli Kohli
    Dr. Kamal Kant Kohli Kohli
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