Technicon Instruments Corp.

Technicon Instruments Corp. — FDA 510(k) Submissions

Technicon Instruments Corp. has submitted 157 FDA 510(k) premarket notifications since 1976, of which 156 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Analyzer, Chemistry (sequential Multiple, Continuous Flow) Clinical Use, Counter, Cell, Automated (particle Counter), Counter, Differential Cell, Photometric Method, Magnesium, Nadh Oxidation/nad Reduction, Alt/sgpt . Use the specialty filter in the sidebar to narrow results.