# Getemed Medizin- Und Informationstechnik AG

- Location (FDA's records): Great Neck, NY
- FDA decisions: 8 (2005–2017): 8 510(k) clearances
- Product codes: DQK (4), MWJ (4)
- Predicates its devices cite: 13 (5 its own); citations of its devices by later devices: 6 (5 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ge Medical Systems Information Technologies: 2 (https://510kreport.com/company/ge-medical-systems-information-technologies)
- North East Monitoring, Inc.: 2 (https://510kreport.com/company/north-east-monitoring)
- Rozinn Electronics, Inc.: 2 (https://510kreport.com/company/rozinn-electronics)
- Mortara Instrument, Inc.: 1 (https://510kreport.com/company/mortara-instrument)
- Card Guard Scientific Survival, Ltd.: 1 (https://510kreport.com/company/card-guard-scientific-survival)

## Firms that cite its devices most
- Atsens Co., Ltd.: 1 (https://510kreport.com/company/atsens)

## Its most-cited devices
- K063042: Cardiomem CM 3000-12BT (2007), cited by 2
- K162023: CardioDay V2.5 (2017), cited by 1
- K051471: Cardioday (2005), cited by 1
- K130516: Cardioday (2013), cited by 1
- K070280: Cardioday, Version 2.0 (2007), cited by 1

## Recent decisions
- K162023: CardioDay V2.5 (Mar 24, 2017)
- K130516: Cardioday (Aug 23, 2013)
- K130785: SEER 1000 (Jul 26, 2013)
- K122272: Cardiomem (Mar 28, 2013)
- K063042: Cardiomem CM 3000-12BT (May 30, 2007)
- K070280: Cardioday, Version 2.0 (Feb 23, 2007)
- K051686: Cardiomem CM 3000-12 (Jul 14, 2005)
- K051471: Cardioday (Jun 29, 2005)

Source page: https://510kreport.com/company/getemed-medizin-und-informationstechnik