The FDA approval focuses on an alert for urgent findings of
pneumothorax, which the company said has demonstrated potential to
reduce turnaround time and increase the radiologist’s confidence in
making this diagnosis.Pneumothorax is an accumulation of gas within
the space between the lung and the chest wall that can lead to total
lung collapse. It is usually diagnosed by chest X-ray scan but is
difficult to interpret.
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Misdiagnosis or late diagnosis of pneumothorax impacts around 74,000
Americans per year, the company said.Zebra has raised $50 million
and its lead investor is the aMoon2 healthtech fund, founded by Yair
Schindel and Marius Nacht. Other investors are Khosla Ventures, Marc
Benioff, Intermountain Investment Fund, OurCrowd Qure, Aurum, Nvidia,
Johnson & Johnson and Dolby Ventures.
(Reporting by Tova Cohen; Editing by Ari Rabinovitch)
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