Acumedia Manufacturers, Inc.

Acumedia Manufacturers, Inc. — FDA 510(k) Submissions

Acumedia Manufacturers, Inc. has submitted 177 FDA 510(k) premarket notifications since 1981, of which 177 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Culture Media, Non-selective And Non-differential, Culture Media, Selective And Differential, Culture Media, Selective And Non-differential, Culture Media, Non-selective And Differential, Supplement, Culture Media . Use the specialty filter in the sidebar to narrow results.