Dynarad Corp.

Dynarad Corp. — FDA 510(k) Submissions

Dynarad Corp. has submitted 9 FDA 510(k) premarket notifications since 1993, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, X-ray, Mobile, Unit, X-ray, Extraoral With Timer, System, X-ray, Mammographic, Collimator, Manual, Radiographic, Assembly, Tube Housing, X-ray, Diagnostic . Use the specialty filter in the sidebar to narrow results.