# Avecor Cardiovascular, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 9 (1993–1998): 9 510(k) clearances
- Product codes: DTN (3), DTZ (2), DWF (1), DTQ (1), KRJ (1), DTM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 25 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtronic, Inc.: 8 (https://510kreport.com/company/medtronic)
- Medtronic Perfusion Systems: 7 (https://510kreport.com/company/medtronic-perfusion-systems)
- Medtronic Vascular: 5 (https://510kreport.com/company/medtronic-vascular)
- Lifebridge Medizintechnik AG: 2 (https://510kreport.com/company/lifebridge-medizintechnik)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Jostra Bentley: 1 (https://510kreport.com/company/jostra-bentley)
- Tyco Healthcare Group LP: 1 (https://510kreport.com/company/tyco-healthcare-group)

## Its most-cited devices
- K973760: Affinity Hollow Fiber Oxygenator with Trillium Biopassive Surface (1998), cited by 11
- K932252: Affinity Hollow Fiber Oxygenator (1993), cited by 3
- K936003: Affinity CVR (1994), cited by 3
- K952532: Affinity Arterial Blood Filter (1995), cited by 3
- K971105: Myotherm (TM) XP Cardioplegia Delivery System (1997), cited by 2
- K935717: Affinity Venous Reservior Bag (1994), cited by 2

## Recent decisions
- K973760: Affinity Hollow Fiber Oxygenator with Trillium Biopassive Surface (Feb 18, 1998)
- K964017: Affinity Blood Pump System (Aug 5, 1997)
- K971105: Myotherm (TM) XP Cardioplegia Delivery System (Jul 11, 1997)
- K952532: Affinity Arterial Blood Filter (Oct 6, 1995)
- K940126: Avecor Pre-Bypass Filter (Jun 28, 1994)
- K936003: Affinity CVR (Jun 20, 1994)
- K935717: Affinity Venous Reservior Bag (May 10, 1994)
- K932252: Affinity Hollow Fiber Oxygenator (Nov 19, 1993)

Source page: https://510kreport.com/company/avecor-cardiovascular