Oldelft Corp. of America

Oldelft Corp. of America — FDA 510(k) Submissions

Oldelft Corp. of America has submitted 9 FDA 510(k) premarket notifications since 1989, of which 9 received clearance as substantially equivalent to a predicate device.

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