The US Food and Drug Administration (FDA) has granted 510(k) clearance for GE Healthcare’s artificial intelligence (AI) algorithm that helps in assessing endotracheal tube (ETT) placements in chest x-ray images.

The algorithm is said to be one of five solutions included in the company’s Critical Care Suite 2.0.

This suite includes AI algorithms embedded on a mobile x-ray device to help radiologists prioritise critical cases and reduce review time by automating the process.

The company stated that the Critical Care Suite 2.0 automatically detects ETTs in chest x-ray images.

It is designed to display an accurate measurement of the tube positioning on the monitor of the x-ray system within seconds.

The measurements can be accessed and reviewed in picture archiving and communication systems (PACS). This will help in determining if the ETT is placed correctly or requires additional attention.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Notably, inaccurate placement of ETT can trigger various complications, including a type of collapsed lung known as pneumothorax.

However, the Critical Care Suite 2.0 can issue an automated alert to radiologists for suspected pneumothorax cases. Additionally, an on-device notification is sent to the technologist regarding the prioritised cases.

Since November 2020, GE Healthcare has been distributing Critical Care Suite 2.0 under the FDA’s Covid-19 imaging guidance.

The company stated that the new clearance will allow the system to be used separately from the public health emergency.

GE Healthcare imaging president and CEO Jan Makela said: “At GE Healthcare, we saw the potential role of Critical Care Suite 2.0 in helping hospitals manage the crisis caused by the number of patients who needed ETT placements during the pandemic, requiring accelerated innovation, and we quickly worked with the FDA to make the solution available to clinicians.

“GE Healthcare is not only accelerating the development and access of new tools to help hospital staff keep up with demand, but also leading the way on Covid-era advancements that will transform the industry and have a long-lasting impact after the pandemic.”