E K Ind., Inc.

E K Ind., Inc. — FDA 510(k) Submissions

E K Ind., Inc. has submitted 50 FDA 510(k) premarket notifications since 1984, of which 49 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Products, Red-cell Lysing Products, Stain, Papanicolau, Formulations, Balanced Salt Solutions, Ph Buffer, Reagent, Schiff . Use the specialty filter in the sidebar to narrow results.