FDA grants 510(k) clearance to AI-based lung segmentation software

The FDA has granted 510(k) clearance to LungQ 3.0.0, an artificial intelligence-based software that identifies different parts of lung anatomy and evaluates lung tissue and fissure completeness, according to a press release.
With use of this version of LungQ (Thirona), the release said physicians will feel supported when diagnosing and documenting pulmonary tissue images since the software identifies and separates pulmonary segments and subsegments.
“The FDA 510(k) clearance for Thirona’s LungQ version 3.0.0 Software translates to more personalized and localized treatment of patients,”

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