Cair Lgl

Cair Lgl — FDA 510(k) Submissions

Cair Lgl has submitted 8 FDA 510(k) premarket notifications since 2014, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Set, Administration, Intravascular, Gastrointestinal Tubes With Enteral Specific Connectors, Enteral Specific Transition Connectors, Enteral Syringes With Enteral Specific Connectors . Use the specialty filter in the sidebar to narrow results.