Prodesse, Inc.

Prodesse, Inc. — FDA 510(k) Submissions

Prodesse, Inc. has submitted 6 FDA 510(k) premarket notifications since 2008, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Respiratory Virus Panel Nucleic Acid Assay System, Human Metapneumovirus (hmpv) Rna Assay System, Reagents, Clostridium Difficile Toxin, Parainfluenza Multiplex Nucleic Acid Assay . Use the specialty filter in the sidebar to narrow results.