Hemocue AB

Hemocue AB — FDA 510(k) Submissions

Hemocue AB has submitted 6 FDA 510(k) premarket notifications since 2006, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Hemoglobin, Automated, Automated Urinalysis System, Glucose Dehydrogenase, Glucose, Counter, Cell, Automated (particle Counter) . Use the specialty filter in the sidebar to narrow results.