# K880103: Catheter, Cannula and Tubing, Vascular, Cardiopul.

- Pathway: 510(k) (Traditional)
- Applicant: Research Medical, Inc.
- Decided: Mar 22, 1988 after 70 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 7 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K991170: Retrograde Cardioplegia Cannula with Duraflo Treatment, Model Dii-RC-014 (1999), 1 descendant of its own
- K123187: Retrograde Coronary Sinus Cardioplegia Catheter, Retrograde Cardioplegia Catheter, Retrograde Cardioplegia Cannula (2013), 0 descendants of its own
- K041739: Edwards E360 Surgical Ablation Device (2004), 0 descendants of its own
- K983791: Peripheral Retrograde Cardiaplegia Cannula (1999), 0 descendants of its own
- K964393: Chase Retrograde Cardioplegia Cannula (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K880103
Methodology: https://510kreport.com/methodology