# K002892: Frsenius PD Iqcard Cycler

- Pathway: 510(k) (Traditional)
- Applicant: Fresenius Medical Care North America
- Decided: Apr 5, 2001 after 202 days
- Product code: FKX (System, Peritoneal, Automatic Delivery)
- Device class: 2
- Regulation: 21 CFR 876.5630
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 2 cite it directly.
0 of 16 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
- K043363: Fresenius Liberty Cycler (2005), 13 descendants of its own
- K123630: Fresenius Liberty Cycler (2013), 6 descendants of its own
- K141145: Liberty PDX Cycler (2014), 5 descendants of its own
- K171652: Fresenius Liberty Select Cycler (2017), 4 descendants of its own
- K181108: Fresenius Liberty Select Cycler (2018), 3 descendants of its own

## Recalls of this device
- Mar 22, 2006 · Not classified · Z-0834-06: Stay safe trigger body may not connect to the extension set and result in associated peritonitis

Source page: https://510kreport.com/device/K002892
Methodology: https://510kreport.com/methodology