Corning Costar Corp.

Corning Costar Corp. — FDA 510(k) Submissions

Corning Costar Corp. has submitted 8 FDA 510(k) premarket notifications since 1980, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Microtiter Diluting/dispensing, Device, General Purpose, Microbiology, Diagnostic, Flask, Tissue Culture, Set, I.v. Fluid Transfer . Use the specialty filter in the sidebar to narrow results.