# K962707: Minntech Minnifilter Plus Hemofilter and Tubing Set

- Pathway: 510(k) (Traditional)
- Applicant: Minntech Corp.
- Decided: Oct 9, 1996 after 89 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K071298: HF Junior Hemofilter (2007), 1 descendant of its own
- K123395: Nxstage System One Low Volume Cartridge Express (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K962707
Methodology: https://510kreport.com/methodology