ZOLL Medical Corporation

ZOLL Medical Corporation — FDA 510(k) Submissions

ZOLL Medical Corporation has submitted 30 FDA 510(k) premarket notifications since 2005, of which 30 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automated External Defibrillators (non-wearable), Display, Cathode-ray Tube, Medical, Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms), Ventilator, Continuous, Facility Use, Dc-defibrillator, Low-energy, (including Paddles) . Use the specialty filter in the sidebar to narrow results.