# Edwards Lifesciences Research Medical

- Location (FDA's records): Midvale, UT
- FDA decisions: 6 (1998–2008): 6 510(k) clearances
- Product codes: DWF (4), DQR (1), DTM (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 4 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Research Medical, Inc.: 3 (https://510kreport.com/company/research-medical)
- Baxter Healthcare Corp: 1 (https://510kreport.com/company/baxter-healthcare)
- Integra Neurocare, LLC: 1 (https://510kreport.com/company/integra-neurocare)
- Research Industries Corp.: 1 (https://510kreport.com/company/research-industries)

## Firms that cite its devices most
- Edwards Lifesciences, LLC: 2 (https://510kreport.com/company/edwards-lifesciences)
- Cardiogard Medical, Ltd.: 1 (https://510kreport.com/company/cardiogard-medical)
- Jms North America Corp.: 1 (https://510kreport.com/company/jms-north-america)
- Endoscopic Technologies, Inc. D/B/A Estech: 1 (https://510kreport.com/company/endoscopic-technologies-d-b-a-estech)
- A-Med Systems, Inc.: 1 (https://510kreport.com/company/a-med-systems)

## Its most-cited devices
- K974259: Venous Flex II Peripheral and Intra-Operative Access Venous Return Cannulae (1998), cited by 2
- K991170: Retrograde Cardioplegia Cannula with Duraflo Treatment, Model Dii-RC-014 (1999), cited by 1
- K990396: T-Anastaflo (1999), cited by 1
- K073559: 18 FR. Rmi Arterial Perfusion Cannula II, 20 FR. Rmi Arterial Perfusion Cannula II (2008), cited by 1
- K062429: Modification to Embol-X Intra-Aortic Filter: X-Small, Small, Medium, Large, X-Large with Heparin Coated Mesh (2006), cited by 1

## Recent decisions
- K073559: 18 FR. Rmi Arterial Perfusion Cannula II, 20 FR. Rmi Arterial Perfusion Cannula II (Jan 31, 2008)
- K062429: Modification to Embol-X Intra-Aortic Filter: X-Small, Small, Medium, Large, X-Large with Heparin Coated Mesh (Sep 27, 2006)
- K990396: T-Anastaflo (Oct 1, 1999)
- K991170: Retrograde Cardioplegia Cannula with Duraflo Treatment, Model Dii-RC-014 (Jul 2, 1999)
- K983791: Peripheral Retrograde Cardiaplegia Cannula (Jun 11, 1999)
- K974259: Venous Flex II Peripheral and Intra-Operative Access Venous Return Cannulae (Dec 1, 1998)

Source page: https://510kreport.com/company/edwards-lifesciences-research-medical