Rusch Intl.

Rusch Intl. — FDA 510(k) Submissions

Rusch Intl. has submitted 43 FDA 510(k) premarket notifications since 1995, of which 43 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tube, Tracheal (w/wo Connector), Tube Tracheostomy And Tube Cuff, Tubes, Gastrointestinal (and Accessories), Catheter, Retention Type, Balloon, Device, Cystometric, Hydraulic . Use the specialty filter in the sidebar to narrow results.