Impra, Inc.

Impra, Inc. — FDA 510(k) Submissions

Impra, Inc. has submitted 29 FDA 510(k) premarket notifications since 1979, of which 24 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Vascular Graft, Of 6mm And Greater Diameter, Prosthesis, Vascular Graft, Of Less Then 6mm Diameter, Apparatus, Autotransfusion, Catheter, Subclavian, Tubes, Gastrointestinal (and Accessories) . Use the specialty filter in the sidebar to narrow results.