GE Healthcare’s Critical Care Suite AI-Powered X-ray Device Receives FDA’s 510(k) Clearance to Identify Pneumothorax

 GE Healthcare’s Critical Care Suite AI-Powered X-ray Device Receives FDA’s 510(k) Clearance to Identify Pneumothorax

GE Healthcare’s Critical Care Suite AI Powered X-ray Device Receives FDA’s 510(k) Clearance to Identify Pneumothorax

Shots:

  • GE Healthcare’s Critical Care Suite reduces the detection time of a collapsed lung from 8hrs. to 15min by utilizing AI algorithm to analyze images from an X-ray
  • GE Healthcare built its device in collaboration with UC San Francisco, which in the suspected case sent images directly to the radiologist for review via picture archiving and communication systems and provide an on-device notification to give awareness of the prioritized cases
  • The device utilizes GE Healthcare’s Edison platform, deployed on its Optima XR240amx system and offers AI quality check features to detect acquisition errors, flagging images for technologist review

Click here to­ read full press release/ article | Ref: GE Healthcare | Image: The Business Journals

Tuba Khan

Tuba Khan is Senior Editor at PharmaShots. She is curious, creative, and passionate about recent updates and innovation in the Life sciences industry. She covers Biopharma, MedTech, and Digital health segments. Tuba also has an experience of digital and social media marketing and runs the campaigns independently. She can be contacted on tuba@pharmashots.com

Related post