Verichem Laboratories, Inc.

Verichem Laboratories, Inc. — FDA 510(k) Submissions

Verichem Laboratories, Inc. has submitted 14 FDA 510(k) premarket notifications since 1988, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Calibrator, Multi-analyte Mixture, Calibrators, Drug Mixture, Calibrator, Primary, Enzyme Controls (assayed And Unassayed), Calibrator, Secondary . Use the specialty filter in the sidebar to narrow results.