Agilent Technologies, Inc.
Agilent Technologies, Inc. — FDA 510(k) Submissions
Agilent Technologies, Inc. has submitted 30 FDA 510(k) premarket notifications since 1985, of which 30 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms), Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms), Automated External Defibrillators (non-wearable), Detector And Alarm, Arrhythmia, System, Imaging, Pulsed Doppler, Ultrasonic . Use the specialty filter in the sidebar to narrow results.