Poly Medicure Limited

Poly Medicure Limited — FDA 510(k) Submissions

Poly Medicure Limited has submitted 5 FDA 510(k) premarket notifications since 2023, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Set, Administration, Intravascular . Use the specialty filter in the sidebar to narrow results.