Millipore Corp.

Millipore Corp. — FDA 510(k) Submissions

Millipore Corp. has submitted 30 FDA 510(k) premarket notifications since 1977, of which 30 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrumentation, High Pressure Liquid Chromatography, Unit, Filter, Membrane, Apparatus, High Pressure Liquid Chromatography, Filter, Conduction, Anesthetic, Filter, Infusion Line . Use the specialty filter in the sidebar to narrow results.