Volu Sol Medical Industries

Volu Sol Medical Industries — FDA 510(k) Submissions

Volu Sol Medical Industries has submitted 66 FDA 510(k) premarket notifications since 1979, of which 66 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Hematoxylin, System, Multipurpose For In Vitro Coagulation Studies, Stain, Papanicolau, Alkaline Picrate, Colorimetry, Creatinine, Instrument, Coagulation . Use the specialty filter in the sidebar to narrow results.