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# FDA Clears GE Critical Care Suite 2.1
- URL: https://www.fdaweb.com/fda-clears-ge-critical-care-suite-2-1/
- Published: 2023-11-30T12:00:00.000Z
- Updated: 2026-09-14T14:17:25.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5155896

FDA has given 510(k) clearance to GE Healthcare’s Critical Care Suite 2.1 featuring a pneumothorax (PTX) algorithm for the detection, notification, triage, and diagnosis of PTX. The company [says](https://www.gehealthcare.com/about/newsroom/press-releases/ge-healthcare-expands-on-device-triage-capabilities-of-critical-care-suite-with-fda-clearance-of-algorithm-for-pneumothorax-detection-notification-triage-and-diagnosis?ref=fdaweb.com) the updated PTX algorithm expands the suite’s on-device triage capabilities by providing immediate notification of the presence or absence of pneumothorax, as well as an overlay display both on device and in PACS (picture archiving and communication) to assist with PTX localization.