FDA 510(k) clearance of latest Philips IntelliVue patient monitor software helps drive alarm management strategies toward a more peaceful, healing environment for patients and caregivers Amsterdam, ...
Royal Philips has designed a new FDA-cleared and CE mark approved mobile app, called IntelliVue GuardianSoftware, that gives clinicians updates on a patient’s condition and deterioration. The latest ...
Philips’ IntelliVue Patient Monitors MX750/MX850, IntelliVue 4-Slot Module Rack FMX-4 and IntelliVue Active Displays AD75/AD85 receive FDA Emergency Use Authorization for use in the US during the ...
More than a year after doling out an emergency use authorization for a handful of Philips’ IntelliVue patient monitoring devices, the FDA is doubling down on the regulatory nod. Two of the patient ...
Covidien has announced the launch of its Nellcor SpO2 single parameter module for use with the Philips IntelliVue patient monitoring platform, according to a news release. The Nellcor SpO2 module ...
Amsterdam, the Netherlands - Philips Medical Systems has announced FDA market clearance for its IntelliVue Patient Monitoring System, a device that allows doctors to be at the patient's bedside and ...
Philips PHG recently announced the wide availability of its ambulatory cardiac monitoring service in Spain. The service is brought together by integrating its wearable ePatch device with its AI-driven ...
A year after they were given an emergency nod to be used during the pandemic, two of Royal Philips’ newest patient monitors now are cleared by the Food and Drug Administration. The agency recently ...
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