Zoll Medical Corporation, World Wide Headquarters

Zoll Medical Corporation, World Wide Headquarters — FDA 510(k) Submissions

Zoll Medical Corporation, World Wide Headquarters has submitted 21 FDA 510(k) premarket notifications since 2007, of which 21 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automated External Defibrillators (non-wearable), Dc-defibrillator, Low-energy, (including Paddles), Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm), System, Network And Communication, Physiological Monitors . Use the specialty filter in the sidebar to narrow results.