News Related to Pneumonia

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Breath Diagnostics’ OneBreath Platform Receives FDA Breakthrough Device Designation

Apr 14, 2026

Breath Diagnostics said the FDA granted Breakthrough Device Designation to its OneBreath platform for pre-operative assessment of postoperative pneumonia risk in adults undergoing elective cardiac surgery. The single-breath test analyzes exhaled volatile organic compounds using LC-MS and is intended for use with clinical evaluation and standard risk assessment tools.

WHO, CARB-X, and FDA Take Action on Antibiotic Resistance Crisis

Mar 13, 2026

The World Health Organization published blueprints for urgently needed antibiotics targeting drug-resistant infections, while CARB-X awarded $1.2 million for novel antibiotic research and the FDA issued guidance on antibiotic duration limits in livestock.