CMS is considering a proposed quality measure that would require “appropriate monitoring of patients receiving [patient-controlled analgesia].” This measure seeks to address the high number of errors ...

Expanding the long-running partnership will bring Medtronic technologies, such as the Nellcor pulse oximetry product, to more ...

Although use of pulse oximetry in hospitalized children with respiratory infections is common, the data supporting its use are limited. Recommendations from the American Academy of Pediatrics in 2006 ...

EarlySense, a patient care device maker, has received FDA clearance for its bedside system and central display with oximetry integration, according to AZ Sensors. The system is a continuous patient ...

Treatment guided by cerebral oximetry monitoring for the first 72 hours after birth failed to improve survival for extremely preterm infants, the SafeBoosC-III trial found. At 36 weeks postmenstrual ...

IRVINE, Calif.--(BUSINESS WIRE)--Masimo (NASDAQ:MASI) announced today FDA 510(k) clearance for the pediatric indication for O3™ regional oximetry with the O3 pediatric sensor. Regional oximetry, also ...

ENGLEWOOD, Colo., Dec. 3, 2024 /PRNewswire/ -- Zynex, Inc (ZYXI). (NASDAQ: ZYXI) ("Zynex", "ZMS", "we" or the "Company"), an innovative medical technology company ...

More than a decade into their partnership, Masimo and GE HealthCare are still finding new ways to combine their respective patient monitoring technologies. In the latest expansion of their ...

Irvine, California-based Masimo Technologies, which makes non-invasive patient monitoring devices and sensors, has received FDA 510(k) clearance for its forehead sensor. The adhesive TFA-1 Forehead ...

NEUCHATEL, Switzerland--(BUSINESS WIRE)--Masimo (NASDAQ: MASI) announced today the CE marking for the pediatric indication for O3™ regional oximetry with the O3 pediatric sensor. Regional oximetry, ...