Eli Lilly and Company

Eli Lilly and Company — FDA 510(k) Submissions

Eli Lilly and Company has submitted 5 FDA 510(k) premarket notifications since 2006, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Syringe, Piston, Calculator, Drug Dose, Injection Data Capture Device . Use the specialty filter in the sidebar to narrow results.