MobiHealthNews

FDA clears Masimo’s forehead sensor for pulse oximetry monitoring

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 ...

Medtronic Receives FDA Clearance for Nellcor(TM) Pulse Oximetry System With Nell-EQ(TM) Intelligent Processor, a New Technology Designed To Improve Reliability Across Diverse ...

This regulatory milestone follows news from earlier this year, when the company announced positive verification study results for its Nellcor™ pulse oximetry system with Nell-EQ™ intelligent processor ...
GlobalData on MSN

Masimo secures FDA approval for OIRD detection on wearable patient monitor

The newly cleared capability uses AI through the smartSET pulse oximetry sensor platform.
FierceBiotech

Masimo wins de novo clearance to add oxygen reserve index calculations to pulse oximeters

Stateside, the ORi sensor will be available in several of Masimo’s RD Rainbow pulse oximetry devices: a newly launched one that features four LED sensors and can calculate both oxygen saturation and ...
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, ...
Medscape

Class I Recall of GE Healthcare TruSignal SpO2 Sensors

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 ...