Infusion Technology Intl.

Infusion Technology Intl. — FDA 510(k) Submissions

Infusion Technology Intl. has submitted 3 FDA 510(k) premarket notifications since 1994, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pump, Infusion Or Syringe, Extra-luminal, Pump, Infusion, Set, Administration, Intravascular . Use the specialty filter in the sidebar to narrow results.