# K926373: Altra Flux 200 Hemodialyzer

- Pathway: 510(k) (Traditional)
- Applicant: Althin Medical AB an Affiliate of Baxter Intl
- Decided: Feb 13, 1995 after 783 days
- Product code: KDI (Dialyzer, High Permeability With Or Without Sealed Dialysate System)
- Device class: 2
- Regulation: 21 CFR 876.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K992573: AF-220 Hemodialyzer (2000), 2 descendants of its own
- K013550: Clirans E-Series Dialyzer (2001), 1 descendant of its own
- K162248: Asahi ViE-U Series Dialyzer (2017), 0 descendants of its own
- K970679: Altra Flux 200 Hemodialyzer (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K926373
Methodology: https://510kreport.com/methodology