Cedic S.R.L.

Cedic S.R.L. — FDA 510(k) Submissions

Cedic S.R.L. 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 Enteral Specific Transition Connectors, Gastrointestinal Tubes With Enteral Specific Connectors, Set, Administration, Intravascular, Tubes, Gastrointestinal (and Accessories) . Use the specialty filter in the sidebar to narrow results.