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Zdrowie i gospodarka · 13/12/2002

FDA Publishes Draft Guidance for Arrhythmia Detector and Alarm Device

The FDA has released a draft guidance document outlining special controls for the arrhythmia detector and alarm device, which is set to be reclassified from class III to class II, pending a proposed rule published in the Federal Register.

Source: Federal Register — Food and Drug AdministrationOpen original release →