Ekf Diagnostic GmbH

Ekf Diagnostic GmbH — FDA 510(k) Submissions

Ekf Diagnostic GmbH has submitted 5 FDA 510(k) premarket notifications since 2003, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Hemoglobin, Automated, Assay, Glycosylated Hemoglobin . Use the specialty filter in the sidebar to narrow results.