Union Carbide Corp.

Union Carbide Corp. — FDA 510(k) Submissions

Union Carbide Corp. has submitted 69 FDA 510(k) premarket notifications since 1976, of which 69 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Liquid-oxygen, Portable, Analyzer, Chemistry, Centrifugal, For Clinical Use, Camera, Scintillation (gamma), Calibrator, Secondary, Station, Pipetting And Diluting, For Clinical Use . Use the specialty filter in the sidebar to narrow results.