FDA Clears Getinge Edi Catheter
The FDA granted 510(k) clearance to Getinge's 6Fr/48 cm Edi catheter designed for premature infants weighing between 500 and 1,000 grams.
The FDA granted 510(k) clearance to Getinge's 6Fr/48 cm Edi catheter designed for premature infants weighing between 500 and 1,000 grams.
The inaugural honor from the American Society for Radiation Oncology (ASTRO) recognizes longstanding contributions to cancer care technology, education, and clinical research.
For patients in the pediatric ICU, pulse oximetry and waveform capnography are valuable tools to monitor the effectiveness of respiratory support and to inform treatment decisions.
On World Interstitial Lung Disease Day, the American Lung Association launched an initiative to helping PPF patients and caregivers recognize worsening symptoms and lung scarring.
The FDA's Expedited Investigational New Drug (IND) Pilot pairs drug sponsors with research institutions to reduce startup delays for early human studies.
A national survey shows that while most laboratories use oscillometry technology, lack of standardized guidelines and high costs limit its growth.
Deliberate laughter therapy exercises are as effective as traditional breathing techniques for improving symptoms and overall health.