Eurotrol B.V.

Eurotrol B.V. — FDA 510(k) Submissions

Eurotrol B.V. has submitted 7 FDA 510(k) premarket notifications since 2006, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Multi-analyte Controls, All Kinds (assayed), Control, Hemoglobin, Single (specified) Analyte Controls (assayed And Unassayed), Control, Hematocrit, Controls For Blood-gases, (assayed And Unassayed) . Use the specialty filter in the sidebar to narrow results.