Electrophoresis Corp. of America

Electrophoresis Corp. of America — FDA 510(k) Submissions

Electrophoresis Corp. of America has submitted 27 FDA 510(k) premarket notifications since 1978, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrophoretic, Protein Fractionation, Electrophoretic, Lactate Dehydrogenase Isoenzymes, Apparatus, Electrophoresis, For Clinical Use, System, Analysis, Electrophoretic Hemoglobin, Enzyme Controls (assayed And Unassayed) . Use the specialty filter in the sidebar to narrow results.