Exelint International, Co.

Exelint International, Co. — FDA 510(k) Submissions

Exelint International, Co. has submitted 7 FDA 510(k) premarket notifications since 2000, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Hypodermic, Single Lumen, Set, Administration, Intravascular, Needle, Fistula, Set, I.v. Fluid Transfer, Syringe, Piston . Use the specialty filter in the sidebar to narrow results.