Zdrowie i gospodarka · 08/03/2004

FDA Corrects Final Rule on Arrhythmia Detector and Alarm Devices

The Food and Drug Administration (FDA) is correcting a final rule that incorrectly reclassified arrhythmia detector and alarm devices from class III to class II, a move that affects devices used to monitor electrocardiograms and produce signals or alarms for atrial or ventricular arrhythmias.