Immunicon Corp.

Immunicon Corp. — FDA 510(k) Submissions

Immunicon Corp. has submitted 6 FDA 510(k) premarket notifications since 2002, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Immunomagnetic, Circulating Cancer Cell, Enumeration, Apparatus, Automated Blood Cell Diluting, Counter, Differential Cell, Tubes, Vials, Systems, Serum Separators, Blood Collection . Use the specialty filter in the sidebar to narrow results.