Diemolding Corp.

Diemolding Corp. — FDA 510(k) Submissions

Diemolding Corp. has submitted 12 FDA 510(k) premarket notifications since 1976, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spirometer, Therapeutic (incentive), Apparatus, Autotransfusion, Nebulizer, Medicinal, Non-ventilatory (atomizer), System, Simulation, Radiation Therapy, Mixer, Cement, For Clinical Use . Use the specialty filter in the sidebar to narrow results.