Echocath, Inc.

Echocath, Inc. — FDA 510(k) Submissions

Echocath, Inc. has submitted 6 FDA 510(k) premarket notifications since 1993, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Transducer, Ultrasonic, Wire, Guide, Catheter, System, Imaging, Pulsed Doppler, Ultrasonic, Catheters, Salpingography, Catheter, Electrode Recording, Or Probe, Electrode Recording . Use the specialty filter in the sidebar to narrow results.