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Unapproved device concerns FDA raised concerns about Zoll's RescueNet Live software, stating that if the software analyzes data from a monitoring device and generates a secondary alarm and is not merely receiving and displaying alarms, then it is a medical device and is adulterated because Zoll "does not have an approved application for premarket approval (PMA) in effect." Company responses Zoll submitted multiple responses between May 2025 and April 2026 from various quality assurance personnel
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