Sekisui Diagnostics P.E.I., Inc.

Sekisui Diagnostics P.E.I., Inc. — FDA 510(k) Submissions

Sekisui Diagnostics P.E.I., Inc. has submitted 6 FDA 510(k) premarket notifications since 2011, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Colorimetry, Acetaminophen, Photometric Method, Magnesium, Calibrator, Secondary, Hemoglobin A1c Test System, Nad Reduction/nadh Oxidation, Cpk Or Isoenzymes . Use the specialty filter in the sidebar to narrow results.