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Business · 22/09/2000

FDA Releases Draft Guidance for Infant/Child Apnea Monitor 510(k) Submissions

The US Food and Drug Administration (FDA) has published a draft guidance document outlining the minimum requirements for infant/child apnea monitors, with the aim of ensuring the safety and effectiveness of these devices for patients of all ages.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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