Logos Scientific, Inc.

Logos Scientific, Inc. — FDA 510(k) Submissions

Logos Scientific, Inc. has submitted 9 FDA 510(k) premarket notifications since 1984, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Apparatus, Electrophoresis, For Clinical Use, Densitometer/scanner (integrating, Reflectance, Tlc, Radiochromat.) Clinica, Instrument, Coagulation, Diazo Colorimetry, Bilirubin, Colorimeter, Photometer, Spectrophotometer For Clinical Use . Use the specialty filter in the sidebar to narrow results.