# K900492: Labeling Change - Viaspan (TM) (Belzer UW)

- Pathway: 510(k) (Traditional)
- Applicant: The DU Pont Co.
- Decided: Mar 20, 1990 after 46 days
- Product code: KDL (Set, Perfusion, Kidney, Disposable)
- Device class: 2
- Regulation: 21 CFR 876.5880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 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
- K991594: Celsior Cold Flush, Storage and Transport Solution for Hearts (1999), 9 descendants of its own
- K123326: Sherpa Pak Cardiac Transport System (2013), 6 descendants of its own
- K133694: Sherpa Pak Transporter (2014), 3 descendants of its own
- K133432: Sherpa Pak Cardiac Transport System (2014), 3 descendants of its own
- K180194: SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System (2018), 1 descendant of its own

Source page: https://510kreport.com/device/K900492
Methodology: https://510kreport.com/methodology