Boddingtons Plastics, Ltd.

Boddingtons Plastics, Ltd. — FDA 510(k) Submissions

Boddingtons Plastics, Ltd. has submitted 5 FDA 510(k) premarket notifications since 2012, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscopic Access Overtube, Gastroenterology-urology, Enteroscope And Accessories . Use the specialty filter in the sidebar to narrow results.