Cybersonics, Inc.

Cybersonics, Inc. — FDA 510(k) Submissions

Cybersonics, Inc. has submitted 7 FDA 510(k) premarket notifications since 2005, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Lithotriptor, Electro-hydraulic, Lithotriptor, Ultrasonic . Use the specialty filter in the sidebar to narrow results.