Hematronix, Inc.

Hematronix, Inc. — FDA 510(k) Submissions

Hematronix, Inc. has submitted 9 FDA 510(k) premarket notifications since 1990, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mixture, Hematology Quality Control, Urinalysis Controls (assayed And Unassayed), Multi-analyte Controls, All Kinds (assayed), Control, Cell Counter, Normal And Abnormal . Use the specialty filter in the sidebar to narrow results.