# K882428: REDY 2000

- Pathway: 510(k) (Traditional)
- Applicant: Organon Teknika Corp.
- Decided: Oct 25, 1988 after 134 days
- Product code: FKT (System, Dialysate Delivery, Sorbent Regenerated)
- Device class: 2
- Regulation: 21 CFR 876.5600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K043574: Allient Sorbent Hemodialysis System, Model 1000 (2005), 1 descendant of its own
- K060381: Allient Sorbet Hemodialysis System, Model 1100 (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K882428
Methodology: https://510kreport.com/methodology