Medical Device Manufacturer · US , Great Neck , NY

Getemed Medizin- Und Informationstechnik AG - FDA 510(k) Cleared Devi...

8 submissions · 8 cleared · Since 2005

Recent clearances: CardioDay V2.5, CARDIODAY, SEER 1000

View 8 510(k) Devices ↓
8
Total
8
Cleared
0
Denied

FDA 510(k) Regulatory Record - Getemed Medizin- Und Informationstechnik AG Cardiovascular ✕

8 devices
1-8 of 8
Cleared Mar 24, 2017
CardioDay V2.5
K162023 · DQK
Cardiovascular · 245d
Cleared Aug 23, 2013
CARDIODAY
K130516 · DQK
Cardiovascular · 177d
Cleared Jul 26, 2013
SEER 1000
K130785 · MWJ
Cardiovascular · 127d
Cleared Mar 28, 2013
CARDIOMEM
K122272 · MWJ
Cardiovascular · 241d
Cleared May 30, 2007
CARDIOMEM CM 3000-12BT
K063042 · MWJ
Cardiovascular · 239d
Cleared Feb 23, 2007
CARDIODAY, VERSION 2.0
K070280 · DQK
Cardiovascular · 25d
Cleared Jul 14, 2005
CARDIOMEM CM 3000-12
K051686 · MWJ
Cardiovascular · 21d
Cleared Jun 29, 2005
CARDIODAY
K051471 · DQK
Cardiovascular · 26d
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