Chemicon Intl., Inc.

Chemicon Intl., Inc. — FDA 510(k) Submissions

Chemicon Intl., Inc. has submitted 8 FDA 510(k) premarket notifications since 1995, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antisera, Fluorescent, Coxsackievirus A 1-24, B 1-6, Antisera, Fluorescent, Poliovirus 1-3, Pneumocystis Carinii . Use the specialty filter in the sidebar to narrow results.