# K874650: Peritoneal Dialysis Kit (Acute and Chronic Form)

- Pathway: 510(k) (Traditional)
- Applicant: Quinton, Inc.
- Decided: Dec 9, 1987 after 26 days
- Product code: FKO (Catheter, Peritoneal Dialysis, Single Use)
- Device class: 2
- Regulation: 21 CFR 876.5630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K053123: PD Cath (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K874650
Methodology: https://510kreport.com/methodology