Vital Scientific N.V.

Vital Scientific N.V. — FDA 510(k) Submissions

Vital Scientific N.V. has submitted 5 FDA 510(k) premarket notifications since 1998, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Coagulation, Activated Partial Thromboplastin, Plasma, Coagulation Control, Analyzer, Chemistry, Micro, For Clinical Use, Test, Time, Prothrombin . Use the specialty filter in the sidebar to narrow results.