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 ...
Hoag has entered a 10-year partnership with Royal Philips to standardize and upgrade patient monitoring technology across its hospitals in Orange County, Calif. Here are four things to know about the ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results