Varian Canada, Inc.

Varian Canada, Inc. — FDA 510(k) Submissions

Varian Canada, Inc. has submitted 7 FDA 510(k) premarket notifications since 1991, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Generator, High-voltage, X-ray, Diagnostic, System, X-ray, Mammographic, System, X-ray, Stationary . Use the specialty filter in the sidebar to narrow results.