Across the healthcare landscape, more and more conversations are focusing on health inequity. Specific to pulse oximetry, recent research, media, and regulatory discussions have been raising awareness ...
The longstanding problem of pulse oximeters providing less-accurate readings for people with dark skin tones got another look Friday from a panel of experts for the US Food and Drug Administration.
A Food and Drug Administration advisory committee met Friday to figure out ways to make pulse oximeters more accurate when doing readings on darker skin both in hospitals and at home, after research ...
Michigan Attorney General Dana Nessel joined the attorneys general of 23 other states and the District of Columbia this week in pressing the U.S. Food and Drug Administration to toughen its guidance ...
Acknowledging the disparity in pulse oximetry implicates a $2 billion industry that has faced stricter regulations in recent years in an attempt to address bias in the development and testing of these ...
The FDA grants 510(k) clearance for the use of Masimo's (NASDAQ:MASI) O3 regional oximetry in pediatric patients. Regional oximetry is used in situations where peripheral pulse oximetry (a device is ...
CHICAGO & IRVINE, Calif.--(BUSINESS WIRE)-- GE HealthCare (Nasdaq: GEHC) and Masimo (Nasdaq: MASI) today announced a joint agreement to integrate Masimo Signal Extraction Technology® (SET®) pulse ...
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Sex, but not race, influences obstructive sleep apnea diagnosis when applying the 4% versus 3% scoring rule
Obstructive sleep apnea (OSA) is a common sleep disorder in the U.S. affecting tens of millions, with estimates ranging from 25 to more than 80 million adults. However, most remain unaware they have ...
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