Getemed Medizin- Und Informationstechnik AG

8 FDA 510(k) medical device clearances.

Top product codes for Getemed Medizin- Und Informationstechnik AG

DQK — Cardiovascular 4 devices
MWJ — Cardiovascular 4 devices

Recent clearances by Getemed Medizin- Und Informationstechnik AG

K162023 — CardioDay V2.5 DQK · 2017-03-24
K130516 — CARDIODAY DQK · 2013-08-23
K130785 — SEER 1000 MWJ · 2013-07-26
K122272 — CARDIOMEM MWJ · 2013-03-28
K063042 — CARDIOMEM CM 3000-12BT MWJ · 2007-05-30
K070280 — CARDIODAY, VERSION 2.0 DQK · 2007-02-23
K051686 — CARDIOMEM CM 3000-12 MWJ · 2005-07-14
K051471 — CARDIODAY DQK · 2005-06-29

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