George King Bio-Medical, Inc.

George King Bio-Medical, Inc. — FDA 510(k) Submissions

George King Bio-Medical, Inc. has submitted 5 FDA 510(k) premarket notifications since 1995, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plasma, Coagulation Control, Control, Plasma, Abnormal, Plasma, Coagulation Factor Deficient . Use the specialty filter in the sidebar to narrow results.