# K895199: Biasol Liquid Concentrates, Add'l Acid Concentrate

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Dec 13, 1989 after 117 days
- Product code: KPO (Dialysate Concentrate For Hemodialysis (Liquid Or Powder))
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K041428: Accusol Dialysis Solution (2004), 2 descendants of its own
- K150966: HMB32 (2015), 1 descendant of its own
- K212052: HMB32 Dialysis Solution (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K895199
Methodology: https://510kreport.com/methodology