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Getemed Medizin- Und Informationstechnik AG

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162023CardioDay V2.5March 24, 2017
K130516CARDIODAYAugust 23, 2013
K130785SEER 1000July 26, 2013
K122272CARDIOMEMMarch 28, 2013
K063042CARDIOMEM CM 3000-12BTMay 30, 2007
K070280CARDIODAY, VERSION 2.0February 23, 2007
K051686CARDIOMEM CM 3000-12July 14, 2005
K051471CARDIODAYJune 29, 2005