Pharmacia, Inc.

Pharmacia, Inc. — FDA 510(k) Submissions

Pharmacia, Inc. has submitted 129 FDA 510(k) premarket notifications since 1976, of which 126 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, Radioallergosorbent (rast) Immunological, Ige, Antigen, Antiserum, Control, System, Test, Beta-2-microglobulin Immunological, Colorimeter, Photometer, Spectrophotometer For Clinical Use, Antisera, All Groups, Streptococcus Spp. . Use the specialty filter in the sidebar to narrow results.