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 ...
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 ...
Dutch health tech giant Royal Philips has scored FDA 510(k) clearance for its IntelliVue MX750 and MX850 patient monitors. The monitors, which received an FDA emergency use authorization in 2020 and ...
Opportunity for significant savings in energy consumption, reduction of paper and elimination of disposable batteries for telemetry revealed in Life Cycle Assessment Data from the LCA indicates that ...
SNOQUALMIE, Wash.--(BUSINESS WIRE)--Spacelabs Healthcare ®, a division of OSI Systems, Inc. (the “Company” or “OSI Systems”), and Masimo today announced that they have extended their partnership in ...
Hosted on MSN
Backdoor uncovered in China-made patient monitors — Contec CMS8000 raises questions about healthcare device security
The US-based Cybersecurity & Infrastructure Security Agency recently released an investigation report involving three firmware versions used in a patient monitoring system called Contec CMS8000, used ...
FILE PHOTO: Signage is seen outside of FDA headquarters in White Oak, Maryland (Reuters) - The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks ...
Recently Updated comprehensive100-Page Reporton the Multiparameter Patient Monitors Market, this analysis deep dives into market size, share, and industry trends. According to our latest research, the ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback