Synapse Biomedical’s Diaphragm Pacing System Gets FDA Premarket Approval
The FDA granted premarket approval of Synapse Biomedical’s NeuRx Diaphragm Pacing System for use in patients with spinal cord injuries.
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Search Results for: ventilator
FDA Grants Marketing Authorization for System that Monitors Opioid Use Health Risks
The FDA granted marketing authorization for a device that recognizes when someone experiences opioid-induced respiratory depression.
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Getinge Subsidiary’s Intra-Aortic Balloon Pumps Get Class I Recall
Getinge subsidiary Datascope is recalling two types of Intra-Aortic Balloon Pumps due to the possibility of unexpected device shutdown.
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How to Handle Home Medical Equipment Recalls and Alerts
ECRI’s top health tech hazard for 2023 is “Gaps in At-Home Medical Device Recalls.” Confusing safety notifications lead to patient harm, as manufacturers lack visibility into users, causing some to miss critical safety alerts.
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Best Practices for Thwarting Medical Device Cyberattacks
Part of the problem with healthcare cyberattacks is the growing trend of device interconnectedness to the Internet of Medical Things.
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