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Frans van Houten

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Philips says updates are ‘imminent’

July 27, 2021Liz Beaulieu, Editor

AMSTERDAM – Philips could hear back from the U.S. Food and Drug Administration in August about its plans to replace the foam in certain CPAP devices and ventilators, based on a timeline provided during the company’s July 26 conference call to discuss financial results for the second quarter.  Philips filed "multiple packages" of CFR 806 applications for corrections and removals with the FDA in June and CEO Frans van Houten said, based on prior experience, there’s typically...

CPAP, Foam, Food & Drug Administration (FDA), Philips Recall, Ventilator


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