Intracel Corp.

Intracel Corp. — FDA 510(k) Submissions

Intracel Corp. has submitted 5 FDA 510(k) premarket notifications since 1995, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antisera, Cf, Influenza Virus A, B, C, Counter, Differential Cell, Antigen, Cf (including Cf Control), Cytomegalovirus, Reagents, Clostridium Difficile Toxin, Legionella, Spp., Elisa . Use the specialty filter in the sidebar to narrow results.