Jamieson Film Co.

Jamieson Film Co. — FDA 510(k) Submissions

Jamieson Film Co. has submitted 6 FDA 510(k) premarket notifications since 1991, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Processor, Cine Film, System, X-ray, Angiographic, System, Image Processing, Radiological, Table, Radiographic, Tilting . Use the specialty filter in the sidebar to narrow results.