Philips Alerts Customers to Missed Cardiac Telemetry Notifications
Philips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
Philips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
The FDA has granted 510(k) marketing clearance for AgileMD's eCART Clinical Deterioration Suite for assessing patient condition.
The FDA has granted 510(k) market clearance for the Zynex CM-1600 blood and fluid volume monitoring device.Â
Philips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
The FDA granted marketing authorization for a device that recognizes when someone experiences opioid-induced respiratory depression.
Read MoreZephyr AI and KangarooHealth are partnering to provide clinicians with insights to inform treatment decisions for patients.
Read MoreThe FDA granted marketing authorization to Medasense Biometrics’ PMD-200 patient monitor with NOL technology for monitoring nociception.
Read MoreSpacelabs Healthcare agreed to pay $2.5 million to resolve allegations that it overcharged the U.S. for patient monitoring equipment.
Read MoreSmith+Nephew announced that its LEAF Patient Monitoring System received an innovative technology designation.
Read MoreOpticyte’s Cell Oâ‚‚ Patient Monitor has received Breakthrough Device Designation for the continuous monitoring of those at risk of organ failure.
Read MoreMasimo has expanded its HEOS entertainment platform to provide continuous connection to its cloud-based health monitoring platform.