Focus Technologies, Inc.

Focus Technologies, Inc. — FDA 510(k) Submissions

Focus Technologies, Inc. has submitted 5 FDA 510(k) premarket notifications since 2002, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Elisa, Antibody, West Nile Virus, Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-1 . Use the specialty filter in the sidebar to narrow results.