Pulse Medical receives FDA Breakthrough Device Designation for its μFR® system
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The μFR is an angio-based physiological assessment tool without a pressure wire or hyperemic agents. It has a wider range of indications and is more affordable. μFR® can be used throughout the entire PCI procedure, including precise physiology assessment at Pre-PCI, strategy optimization during the operation, outcome and microcirculatory function assessment at Post-PCI.
A device must demonstrate that it has the potential to offer for more efficient treatment or diagnosis of life-threatening or irreversibly debilitating diseases or conditions to be eligible for the Breakthrough Device Designation. The classification enables a coordinated and expedited review process with FDA, accelerating the commercialization of Pulse Medical.
"We are delighted that μFR® has been designated an FDA breakthrough device. "said Bing LIU, the president of Pulse Medical. "Cardiovascular diseases are the leading cause of death globally; an estimated 17.9 million people died from that in 2019. μFR® as a physiological assessment tool could provide more insights to physicians and help more patients have an effective and precise treatment."
The μFR® also have various robust clinical evidence that provides its outcome benefits. The representative FAVOR III China clinical trial shows that according to a 1-year follow-up, μFR® could bring a 35% MACE risk reduction. The patient group guided by μFR® could also gain a better prognostic result, and the result is published in LANCET.
In the future, Pulse Medical will continue to dedicate itself to the pan-vascular field, fostering a new era of precise and intelligent vascular intervention.
For more information about Pulse Medical, Please visit http://en.pulse-imaging.com/
CONTACT: Yiran Duan, Phone: +86-13641283502
View original content:https://www.prnewswire.co.uk/news-releases/pulse-medical-receives-fda-breakthrough-device-designation-for-its-fr-system-301835740.html
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