Biotest Diagnostics Corp.

Biotest Diagnostics Corp. — FDA 510(k) Submissions

Biotest Diagnostics Corp. has submitted 5 FDA 510(k) premarket notifications since 1996, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Epstein-barr Virus, Other, Antisera, Conjugated Fluorescent, Cytomegalovirus . Use the specialty filter in the sidebar to narrow results.