Wellbeing Magazine on MSN
Patient monitoring devices in general practice: A practical guide for GP clinics
Accurate patient monitoring is not an optional extra in general practice. It is a fundamental part of the clinical encounter, ...
GE HealthCare is recalling 7559 TruSignal arterial oxygen saturation (SpO2) sensors because of problems that may reduce defibrillation energy, expose patients to unintended voltage, or give inaccurate ...
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 ...
IRVINE, Calif.--(BUSINESS WIRE)--Masimo (NASDAQ: MASI) announced today FDA clearance of the Rad-G™ Pulse Oximeter, a rugged handheld device that provides clinically proven SET ® pulse oximetry, ...
The newly cleared capability uses AI through the smartSET pulse oximetry sensor platform.
The Fitbit Charge 6, the latest addition to Fitbit's lineup of fitness trackers, has introduced a significant advancement in health monitoring with its built-in blood oxygen saturation (SpO2) feature.
June 8, 2026 /3BL/ – Medtronic, a global leader in healthcare technology, announced FDA 510(k) clearance of its Nellcor™ pulse oximetry system with Nell-EQ™ intelligent processor. The Nell-EQ™ ...
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