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FDA proposes new guidelines to improve pulse oximeter accuracy across different skin tones.
The FDA has proposed new guidelines for pulse oximeter manufacturers to improve device accuracy across different skin tones.
Studies have shown that these devices can be less accurate for people with darker skin, potentially affecting patient care.
The FDA recommends that manufacturers conduct larger, more diverse clinical studies, including at least 150 patients and 25% with darker skin tones, to ensure the devices work effectively for all racial groups.
These changes aim to reduce racial biases in medical technology.
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La FDA propone nuevas pautas para mejorar la precisión del oxímetro de pulso en diferentes tonos de la piel.