Ekf-Diagnostic GmbH

Ekf-Diagnostic GmbH holds 5 FDA 510(k) medical device clearances, first cleared 2003, most recent 2020.

Name variants for Ekf-Diagnostic GmbH

as filed with FDA

Ekf-Diagnostic GmbH4 devices
Ekf Diagnostic GmbH1 device

Top product codes for Ekf-Diagnostic GmbH

GKR — Hematology4 devices
LCP — Hematology1 device

Recent clearances by Ekf-Diagnostic GmbH

K200909 — Hemo Control (optional Add Pack Hemo Control DM)Code GKR·2020-06-12
K180509 — Quo-Test A1c SystemCode LCP·2019-02-16
K172173 — DiaSpect Tm, DiaSpect Tm CuvettesCode GKR·2018-04-06
K110393 — EKF- DIAGNOSTIC HEMO_CONTROL HEMOGLOBIN MEASUREMENT SYSTEM; EKF-DIAGNOSTIC HEMOGLOBIN MICROCUVETTES (MODIFIED CURVETTE WCode GKR·2011-03-04
K031898 — EKF DIAGNOSTIC HEMO CONTROL HEMOGLOBIN MEASUREMENT SYSTEMCode GKR·2003-09-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.