The COVID-19 Airway Management Isolation Chamber system is a barrier device constructed by draping a large clear plastic bag over a box-like frame that is placed over the head, neck, and shoulders of the patient to isolate airborne particulates.
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Amsterdam-based Royal Philips announces that it has received 510(k) clearance from the U.S. FDA to market a wide range of its ultrasound technologies for the management of COVID-19-related lung and cardiac complications.
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With the impact of COVID-19, healthcare organizations may find themselves more vulnerable to cyber threats, especially if they have not prepared well for a crisis. Here are tips from one expert.
Read MoreNow, two new devices could offer additional safety for healthcare workers during the COVID-19 pandemic, while allowing more effective treatment for patients with infections spread by respiratory droplets.
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During COVID-19, the U.S. FDA will continue to utilize and implement additional alternative inspection tools and approaches while postponing domestic and foreign routine surveillance inspections, FDA Commissioner Stephen Hahn, MD, said in a statement.
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