Mesi D.O.O.

Mesi D.O.O. — FDA 510(k) Submissions

Mesi D.O.O. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spirometer, Diagnostic . Use the specialty filter in the sidebar to narrow results.