Cis Radiopharmaceuticals, Inc.

Cis Radiopharmaceuticals, Inc. — FDA 510(k) Submissions

Cis Radiopharmaceuticals, Inc. has submitted 9 FDA 510(k) premarket notifications since 1976, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Radioimmunoassay, Luteinizing Hormone, Radioimmunoassay, Follicle-stimulating Hormone, Set, Oral Administration, Source, Wire, Iridium, Radioactive, Myoglobin, Antigen, Antiserum, Control . Use the specialty filter in the sidebar to narrow results.