Genzyme Corporation

Genzyme Corporation — FDA 510(k) Submissions

Genzyme Corporation has submitted 6 FDA 510(k) premarket notifications since 2005, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Polymeric, Polymer, Ent Synthetic-polyamide (mesh Or Foil Material), Test, Cystatin C, Devices Detecting Influenza A, B, And C Virus Antigens, Reagents, Clostridium Difficile Toxin . Use the specialty filter in the sidebar to narrow results.