Philips Gets 510(k) Clearance for Its Acute Patient Monitors

Philips’s IntelliVue MX750 and IntelliVue MX850 acute patient monitors have received 510(k) clearance from the FDA.

The monitors, which offer enhanced infection prevention in hospitals, can be used with other devices and applications, including Philips’ Patient Information Center iX and IntelliVue XDS software, to display critical patient data remotely or at the point of care, the company said.

The FDA last year granted the monitors Emergency Use Authorization for use by hospitals during the COVID-19 pandemic.