Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Ekf-Diagnostic GmbH

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest Approval2020-06-12
TypeNumberDevice NameCodeDate
510(k) K200909 Hemo Control (optional Add Pack Hemo Control DM) GKR 2020-06-12 View
510(k) K180509 Quo-Test A1c System LCP 2019-02-16 View
510(k) K172173 DiaSpect Tm, DiaSpect Tm Cuvettes GKR 2018-04-06 View
↑