Getemed Medizin- Und Informationstechnik AG is one of 18368 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Getemed Medizin- Und Informationstechnik AG - FDA 510(k) Cleared Devi...
Recent clearances: CardioDay V2.5, CARDIODAY, SEER 1000
8
Total
8
Cleared
0
Denied
Getemed Medizin- Und Informationstechnik AG has 8 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 8 cleared submissions from 2005 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Getemed Medizin- Und Informationstechnik AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Getemed Medizin- Und Informationstechnik AG
8 devices
Cleared
Mar 24, 2017
CardioDay V2.5
Cardiovascular
245d
Cleared
Aug 23, 2013
CARDIODAY
Cardiovascular
177d
Cleared
Jul 26, 2013
SEER 1000
Cardiovascular
127d
Cleared
Mar 28, 2013
CARDIOMEM
Cardiovascular
241d
Cleared
May 30, 2007
CARDIOMEM CM 3000-12BT
Cardiovascular
239d
Cleared
Feb 23, 2007
CARDIODAY, VERSION 2.0
Cardiovascular
25d
Cleared
Jul 14, 2005
CARDIOMEM CM 3000-12
Cardiovascular
21d
Cleared
Jun 29, 2005
CARDIODAY
Cardiovascular
26d