American Bionetics, Inc.

American Bionetics, Inc. — FDA 510(k) Submissions

American Bionetics, Inc. has submitted 3 FDA 510(k) premarket notifications since 1988, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Slide Stainer, Automated, Anti-sm Antibody, Antigen And Control . Use the specialty filter in the sidebar to narrow results.