Fisher Scientific Co., LLC

Fisher Scientific Co., LLC — FDA 510(k) Submissions

Fisher Scientific Co., LLC has submitted 89 FDA 510(k) premarket notifications since 1976, of which 89 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph, Mixture, Hematology Quality Control, Multi-analyte Controls, All Kinds (assayed), Drug Mixture Control Materials, Electrode, Ion Specific, Sodium . Use the specialty filter in the sidebar to narrow results.