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510(k) clearance: Sensinel Cardiopulmonary Management (CPM) System (Analog Devices)

U.S. FDA 510(k) database via openFDA0 comments

Substantially Equivalent on 16 October 2026. Traditional 510(k) K260801. Product code MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)). Cardiovascular panel.

Read the full story at U.S. FDA 510(k) database via openFDA (opens in a new tab)

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Headline and summary from U.S. FDA 510(k) database via openFDA; the full story is on the publisher's site. Nothing here is investment advice.