Lakewood Biochemical Co., Inc.

Lakewood Biochemical Co., Inc. — FDA 510(k) Submissions

Lakewood Biochemical Co., Inc. has submitted 89 FDA 510(k) premarket notifications since 1987, of which 89 received clearance as substantially equivalent to a predicate device.

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