# K222318: Fresenius Liberty Select Cycler

- Pathway: 510(k) (Traditional)
- Applicant: Fresenius Medical Care Renal Therapies Group, LLC
- Decided: Oct 31, 2022 after 90 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
Longest line of descent: 7 generations back to K923065 (1994). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181108: Fresenius Liberty Select Cycler, Fresenius Medical Care Renal Therapies Group, LLC (2018) Summary page 4.

## Recalls of this device
- Oct 24, 2023 · Class III · Z-0619-2024: Affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the clinic.

## Indications for use
The Fresenius Liberty Select Cycler is indicated for acute and chronic peritoneal dialysis.

Source page: https://510kreport.com/device/K222318
Methodology: https://510kreport.com/methodology