Murex Diagnostics Limitd

Murex Diagnostics Limitd — FDA 510(k) Submissions

Murex Diagnostics Limitd has submitted 1 FDA 510(k) premarket notifications since 1995, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Kit, Screening, Staphylococcus Aureus . Use the specialty filter in the sidebar to narrow results.