Immunomedics, Inc.

Immunomedics, Inc. — FDA 510(k) Submissions

Immunomedics, Inc. has submitted 4 FDA 510(k) premarket notifications since 1986, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Complement C3, Antigen, Antiserum, Control, Anti-dna Antibody (enzyme-labeled), Antigen, Control, Anti-sm Antibody, Antigen And Control, Complement C1q, Antigen, Antiserum, Control . Use the specialty filter in the sidebar to narrow results.