Medical Device Manufacturer · US , Annapolis , MD

Zephyr Technology Corporation

4 submissions · 4 cleared · Since 2010
4
Total
4
Cleared
0
Denied

Zephyr Technology Corporation — FDA 510(k) Submissions

Zephyr Technology Corporation has submitted 4 FDA 510(k) premarket notifications since 2010, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms), Transmitters And Receivers, Physiological Signal, Radiofrequency, Electrode, Electrocardiograph . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Cardiovascular 4